Clindamycin Phosphate


Greenstone Llc
Human Prescription Drug
NDC 59762-5009
Clindamycin Phosphate is a human prescription drug labeled by 'Greenstone Llc'. National Drug Code (NDC) number for Clindamycin Phosphate is 59762-5009. This drug is available in dosage form of Cream. The names of the active, medicinal ingredients in Clindamycin Phosphate drug includes Clindamycin Phosphate - 20 mg/g . The currest status of Clindamycin Phosphate drug is Active.

Drug Information:

Drug NDC: 59762-5009
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Clindamycin Phosphate
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Clindamycin Phosphate
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Greenstone Llc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Cream
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:CLINDAMYCIN PHOSPHATE - 20 mg/g
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:VAGINAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: NDA AUTHORIZED GENERIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 11 Aug, 1992
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 27 Jun, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: NDA050680
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Greenstone LLC
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:309337
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UNII:EH6D7113I8
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:Decreased Sebaceous Gland Activity [PE]
Lincosamide Antibacterial [EPC]
Lincosamides [CS]
Neuromuscular Blockade [PE]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
59762-5009-11 TUBE in 1 CARTON (59762-5009-1) / 40 g in 1 TUBE11 Aug, 1992N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Product Elements:

Clindamycin phosphate clindamycin phosphate clindamycin phosphate clindamycin benzyl alcohol cetostearyl alcohol mineral oil polysorbate 60 propylene glycol water sorbitan monostearate stearic acid

Drug Interactions:

Drug interactions systemic clindamycin has been shown to have neuromuscular blocking properties that may enhance the action of other neuromuscular blocking agents. therefore, it should be used with caution in patients receiving such agents.

Indications and Usage:

Indications and usage clindamycin phosphate vaginal cream 2%, is indicated in the treatment of bacterial vaginosis (formerly referred to as haemophilus vaginitis, gardnerella vaginitis, nonspecific vaginitis, corynebacterium vaginitis, or anaerobic vaginosis). clindamycin phosphate vaginal cream 2%, can be used to treat non-pregnant women and pregnant women during the second and third trimester. (see clinical studies .) note: for purposes of this indication, a clinical diagnosis of bacterial vaginosis is usually defined by the presence of a homogeneous vaginal discharge that (a) has a ph of greater than 4.5, (b) emits a "fishy" amine odor when mixed with a 10% koh solution, and (c) contains clue cells on microscopic examination. gram's stain results consistent with a diagnosis of bacterial vaginosis include (a) markedly reduced or absent lactobacillus morphology, (b) predominance of gardnerella morphotype, and (c) absent or few white blood cells. other pathogens commonly associated wit
h vulvovaginitis, eg, trichomonas vaginalis, chlamydia trachomatis, n. gonorrhoeae, candida albicans, and herpes simplex virus should be ruled out.

Warnings:

Warnings pseudomembranous colitis has been reported with nearly all antibacterial agents, including clindamycin, and may range in severity from mild to life-threatening. orally and parenterally administered clindamycin has been associated with severe colitis which may end fatally. diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported with the use of orally and parenterally administered clindamycin, as well as with topical (dermal and vaginal) formulations of clindamycin. therefore, it is important to consider this diagnosis in patients who present with diarrhea subsequent to the administration of clindamycin, even when administered by the vaginal route, because approximately 5% of the clindamycin dose is systemically absorbed from the vagina. treatment with antibacterial agents alters the normal flora of the colon and may permit overgrowth of clostridia. studies indicate that a toxin produced by clostridioides difficile is a primary cause of "an
tibiotic-associated" colitis. after the diagnosis of pseudomembranous colitis has been established, therapeutic measures should be initiated. mild cases of pseudomembranous colitis usually respond to discontinuation of the drug alone. in moderate to severe cases, consideration should be given to management with fluids and electrolytes, protein supplementation, and treatment with an antibacterial drug clinically effective against clostridioides difficile colitis. onset of pseudomembranous colitis symptoms may occur during or after antimicrobial treatment.

General Precautions:

General clindamycin phosphate vaginal cream 2%, contains ingredients that will cause burning and irritation of the eye. in the event of accidental contact with the eye, rinse the eye with copious amounts of cool tap water. the use of clindamycin phosphate vaginal cream 2% may result in the overgrowth of nonsusceptible organisms in the vagina. in clinical studies involving 600 non-pregnant women who received treatment for 3 days, candida albicans was detected, either symptomatically or by culture, in 8.8% of patients. in 9% of the patients, vaginitis was recorded. in clinical studies involving 1325 non-pregnant women who received treatment for 7 days, candida albicans was detected, either symptomatically or by culture, in 10.5% of patients. vaginitis was recorded in 10.7% of the patients. in 180 pregnant women who received treatment for 7 days, candida albicans was detected, either symptomatically or by culture, in 13.3% of patients. in 7.2% of the patients, vaginitis was recorded. cand
ida albicans, as reported here, includes the terms: vaginal moniliasis and moniliasis (body as a whole). vaginitis includes the terms: vulvovaginal disorder, vulvovaginitis, vaginal discharge, trichomonal vaginitis, and vaginitis.

Dosage and Administration:

Dosage and administration the recommended dose is one applicatorful of clindamycin phosphate vaginal cream 2%, (5 grams containing approximately 100 mg of clindamycin phosphate) intravaginally, preferably at bedtime, for 3 or 7 consecutive days in non-pregnant patients and for 7 consecutive days in pregnant patients. (see clinical studies .)

Contraindications:

Contraindications clindamycin phosphate vaginal cream 2%, is contraindicated in individuals with a history of hypersensitivity to clindamycin, lincomycin, or any of the components of this vaginal cream. clindamycin phosphate vaginal cream 2%, is also contraindicated in individuals with a history of regional enteritis, ulcerative colitis, or a history of "antibiotic-associated" colitis.

Adverse Reactions:

Adverse reactions clinical trials non-pregnant women in clinical trials involving non-pregnant women, 1.8% of 600 patients who received treatment with clindamycin phosphate vaginal cream 2% for 3 days and 2.7% of 1325 patients who received treatment for 7 days discontinued therapy due to drug-related adverse events. medical events judged to be related, probably related, possibly related, or of unknown relationship to vaginally administered clindamycin phosphate vaginal cream 2%, were reported for 20.7% of the patients receiving treatment for 3 days and 21.3% of the patients receiving treatment for 7 days. events occurring in ≥1% of patients receiving clindamycin phosphate vaginal cream 2% are shown in table 1. table 1 – events occurring in ≥1% of non-pregnant patients receiving clindamycin phosphate vaginal cream 2% clindamycin phosphate vaginal cream event 3 day n=600 7 day n=1325 urogenital vaginal moniliasis 7.7 10.4 vulvovaginitis 6.0 4.4 vulvovaginal disorder 3.2 5.
3 trichomonal vaginitis 0 1.3 body as a whole moniliasis (body) 1.3 0.2 other events occurring in <1% of the clindamycin vaginal cream 2% groups include: urogenital system: vaginal discharge, metrorrhagia, urinary tract infection, endometriosis, menstrual disorder, vaginitis/vaginal infection, and vaginal pain. body as a whole: localized abdominal pain, generalized abdominal pain, abdominal cramps, halitosis, headache, bacterial infection, inflammatory swelling, allergic reaction, and fungal infection. digestive system: nausea, vomiting, constipation, dyspepsia, flatulence, diarrhea, and gastrointestinal disorder. endocrine system: hyperthyroidism. central nervous system: dizziness and vertigo. respiratory system: epistaxis. skin: pruritus (non-application site), moniliasis, rash, maculopapular rash, erythema, and urticaria. special senses: taste perversion. pregnant women in a clinical trial involving pregnant women during the second trimester, 1.7% of 180 patients who received treatment for 7 days discontinued therapy due to drug-related adverse events. medical events judged to be related, probably related, possibly related, or of unknown relationship to vaginally administered clindamycin phosphate vaginal cream 2%, were reported for 22.8% of pregnant patients. events occurring in ≥1% of patients receiving either clindamycin phosphate vaginal cream 2% or placebo are shown in table 2. table 2 - events occurring in ≥1% of pregnant patients receiving clindamycin phosphate vaginal cream 2% or placebo clindamycin phosphate vaginal cream placebo event 7 day n=180 7 day n=184 urogenital vaginal moniliasis 13.3 7.1 vulvovaginal disorder 6.7 7.1 abnormal labor 1.1 0.5 body as a whole fungal infection 1.7 0 skin pruritus, non-application site 1.1 0 other events occurring in <1% of the clindamycin vaginal cream 2% group include: urogenital system: dysuria, metrorrhagia, vaginal pain, and trichomonal vaginitis. body as a whole: upper respiratory infection. skin: pruritus (topical application site) and erythema. post-marketing experience because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. in the post-marketing period, there have been case reports of pseudomembranous colitis with the use of clindamycin phosphate vaginal cream. other clindamycin formulations clindamycin vaginal cream affords minimal peak serum levels and systemic exposure (aucs) of clindamycin compared to 100 mg oral clindamycin dosing. although these lower levels of exposure are less likely to produce the common reactions seen with oral clindamycin, the possibility of these and other reactions cannot be excluded presently. data from well-controlled trials directly comparing clindamycin administered orally to clindamycin administered vaginally are not available. the following adverse reactions and altered laboratory tests have been reported with the oral or parenteral use of clindamycin: infections and infestations: clostridioides difficile colitis. gastrointestinal: abdominal pain, esophagitis, nausea, vomiting, diarrhea, and pseudomembranous colitis. (see warnings .) hematopoietic: transient neutropenia (leukopenia), eosinophilia, agranulocytosis, and thrombocytopenia have been reported. no direct etiologic relationship to concurrent clindamycin therapy could be made in any of these reports. hypersensitivity reactions: maculopapular rash and urticaria have been observed during drug therapy. generalized mild to moderate morbilliform-like skin rashes are the most frequently reported of all adverse reactions. cases of acute generalized exanthematous pustulosis (agep), erythema multiforme, some resembling stevens-johnson syndrome, have been associated with clindamycin. a few cases of anaphylactoid reactions have been reported. if a hypersensitivity reaction occurs, the drug should be discontinued. liver: jaundice and abnormalities in liver function tests have been observed during clindamycin therapy. musculoskeletal: cases of polyarthritis have been reported. renal: acute kidney injury. immune system: drug reaction with eosinophilia and systemic symptoms (dress) cases have been reported.

Adverse Reactions Table:

TABLE 1 – Events Occurring in ≥1% of Non-pregnant Patients Receiving Clindamycin Phosphate Vaginal Cream 2%
Clindamycin Phosphate Vaginal Cream
Event3 Day n=6007 Day n=1325
Urogenital
Vaginal moniliasis7.710.4
Vulvovaginitis6.04.4
Vulvovaginal disorder3.25.3
Trichomonal vaginitis01.3
Body as a Whole
Moniliasis (body)1.30.2

TABLE 2 - Events Occurring in ≥1% of Pregnant Patients Receiving Clindamycin Phosphate Vaginal Cream 2% or Placebo
Clindamycin Phosphate Vaginal CreamPlacebo
Event7 DAY n=1807 Day n=184
Urogenital
Vaginal moniliasis13.37.1
Vulvovaginal disorder6.77.1
Abnormal labor1.10.5
Body as a Whole
Fungal infection1.70
Skin
Pruritus, non-application site1.10

Drug Interactions:

Drug interactions systemic clindamycin has been shown to have neuromuscular blocking properties that may enhance the action of other neuromuscular blocking agents. therefore, it should be used with caution in patients receiving such agents.

Use in Pregnancy:

Pregnancy teratogenic effects in clinical trials with pregnant women, the systemic administration of clindamycin during the second and third trimesters, has not been associated with an increased frequency of congenital abnormalities. clindamycin vaginal cream should be used during the first trimester of pregnancy only if clearly needed and the benefits outweigh the risks. there are no adequate and well-controlled studies in pregnant women during the first trimester of pregnancy. clindamycin phosphate vaginal cream 2% has been studied in pregnant women during the second trimester. in women treated for seven days, abnormal labor was reported in 1.1% of patients who received clindamycin vaginal cream 2% compared with 0.5% of patients who received placebo. reproduction studies have been performed in rats and mice using oral and parenteral doses of clindamycin up to 600 mg/kg/day (62 and 25 times, respectively, the maximum human exposure based on body surface area) and have revealed no evid
ence of harm to the fetus due to clindamycin. cleft palates were observed in fetuses from one mouse strain treated intraperitoneally with clindamycin at 200 mg/kg/day (about 10 times the recommended dose based on body surface area conversions). since this effect was not observed in other mouse strains or in other species, the effect may be strain specific.

Pediatric Use:

Pediatric use safety and effectiveness in pediatric patients have not been established.

Geriatric Use:

Geriatric use clinical studies for clindamycin phosphate vaginal cream 2% did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. other reported clinical experience has not identified differences in responses between the elderly and younger patients.

Overdosage:

Overdosage vaginally applied clindamycin phosphate vaginal cream 2% could be absorbed in sufficient amounts to produce systemic effects. (see warnings .)

Description:

Description clindamycin phosphate is a water soluble ester of the semi-synthetic antibiotic produced by a 7(s)-chloro-substitution of the 7(r)-hydroxyl group of the parent antibiotic lincomycin. the chemical name for clindamycin phosphate is methyl 7-chloro-6,7,8-trideoxy-6-(1-methyl- trans- 4-propyl-l-2-pyrrolidinecarboxamido)-1-thio-l- threo- α− d-galacto -octopyranoside 2-(dihydrogen phosphate). it has a molecular weight of 504.96, and the molecular formula is c 18 h 34 cln 2 o 8 ps. the structural formula is represented below: clindamycin phosphate vaginal cream 2%, is a semi-solid, white cream, which contains 2% clindamycin phosphate, usp, at a concentration equivalent to 20 mg clindamycin per gram. the ph of the cream is between 3.0 and 6.0. the cream also contains benzyl alcohol, cetostearyl alcohol, mixed fatty acid esters, mineral oil, polysorbate 60, propylene glycol, purified water, sorbitan monostearate, and stearic acid. each applicatorful of 5 grams of vaginal cream contains approximately 100 mg of clindamycin phosphate. chemical structure

Clinical Pharmacology:

Clinical pharmacology mechanism of action clindamycin is an antibacterial drug (see microbiology ) . pharmacokinetics following a once a day intravaginal dose of 100 mg of clindamycin phosphate vaginal cream 2%, administered to 6 healthy female volunteers for 7 days, approximately 5% (range 0.6% to 11%) of the administered dose was absorbed systemically. the peak serum clindamycin concentration observed on the first day averaged 18 ng/ml (range 4 to 47 ng/ml) and on day 7 it averaged 25 ng/ml (range 6 to 61 ng/ml). these peak concentrations were attained approximately 10 hours post-dosing (range 4–24 hours). following a once a day intravaginal dose of 100 mg of clindamycin phosphate vaginal cream 2%, administered for 7 consecutive days to 5 women with bacterial vaginosis, absorption was slower and less variable than that observed in healthy females. approximately 5% (range 2% to 8%) of the dose was absorbed systemically. the peak serum clindamycin concentration observed on the fir
st day averaged 13 ng/ml (range 6 to 34 ng/ml) and on day 7 it averaged 16 ng/ml (range 7 to 26 ng/ml). these peak concentrations were attained approximately 14 hours post-dosing (range 4–24 hours). there was little or no systemic accumulation of clindamycin after repeated vaginal dosing of clindamycin phosphate vaginal cream 2%. the systemic half-life was 1.5 to 2.6 hours. microbiology mechanism of action clindamycin inhibits bacterial protein synthesis by binding to the 23s rna of the 50s subunit of the ribosome. clindamycin is predominantly bacteriostatic. although clindamycin phosphate is inactive in vitro , rapid in vivo hydrolysis converts it to active clindamycin. resistance resistance to clindamycin is most often caused by modification of the target site on the ribosome, usually by chemical modification of rna bases by point mutations in rna or occasionally in proteins. cross resistance has been demonstrated between lincosamides, macrolides and streptogramins b in some organisms. cross resistance has been demonstrated between clindamycin and lincomycin. antibacterial activity culture and sensitivity testing of bacteria are not routinely performed to establish the diagnosis of bacterial vaginosis (see indications and usage ); standard methodology for the susceptibility testing of the potential bacterial pathogens, gardnerella vaginalis, mobiluncus spp., or mycoplasma hominis , has not been defined. the following in vitro data are available but their clinical significance is unknown. clindamycin is active in vitro against most isolates of the following organisms reported to be associated with bacterial vaginosis: bacteroides spp. gardnerella vaginalis mobiluncus spp. mycoplasma hominis peptostreptococcus spp.

Mechanism of Action:

Mechanism of action clindamycin is an antibacterial drug (see microbiology ) .

Pharmacokinetics:

Pharmacokinetics following a once a day intravaginal dose of 100 mg of clindamycin phosphate vaginal cream 2%, administered to 6 healthy female volunteers for 7 days, approximately 5% (range 0.6% to 11%) of the administered dose was absorbed systemically. the peak serum clindamycin concentration observed on the first day averaged 18 ng/ml (range 4 to 47 ng/ml) and on day 7 it averaged 25 ng/ml (range 6 to 61 ng/ml). these peak concentrations were attained approximately 10 hours post-dosing (range 4–24 hours). following a once a day intravaginal dose of 100 mg of clindamycin phosphate vaginal cream 2%, administered for 7 consecutive days to 5 women with bacterial vaginosis, absorption was slower and less variable than that observed in healthy females. approximately 5% (range 2% to 8%) of the dose was absorbed systemically. the peak serum clindamycin concentration observed on the first day averaged 13 ng/ml (range 6 to 34 ng/ml) and on day 7 it averaged 16 ng/ml (range 7 to 26 ng/ml
). these peak concentrations were attained approximately 14 hours post-dosing (range 4–24 hours). there was little or no systemic accumulation of clindamycin after repeated vaginal dosing of clindamycin phosphate vaginal cream 2%. the systemic half-life was 1.5 to 2.6 hours.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility long term studies in animals have not been performed with clindamycin to evaluate carcinogenic potential. genotoxicity tests performed included a rat micronucleus test and an ames test. both tests were negative. fertility studies in rats treated orally with up to 300 mg/kg/day (31 times the human exposure based on mg/m 2 ) revealed no effects on fertility or mating ability.

Clinical Studies:

Clinical studies in two clinical studies involving 674 evaluable non-pregnant women with bacterial vaginosis comparing clindamycin phosphate vaginal cream 2% for 3 or 7 days, the clinical cure rates, determined at 1 month posttherapy, ranged from 72% to 81% for the 3-day treatment and 84% to 86% for the 7-day treatment. clindamycin phosphate vaginal cream 2% 3 day clindamycin phosphate vaginal cream 2% 7 day us study 94/131 72% 110/128 86% european study 161/199 81% 181/216 84% in a clinical study involving 249 evaluable pregnant patients in the second and third trimester treated for 7 days, the clinical cure rate, determined at 1 month posttherapy, was 60% (77/129) in the clindamycin arm and 9% (11/120) for the vehicle arm. the determination of clinical cure was based on the absence of a "fishy" amine odor when the vaginal discharge was mixed with a 10% koh solution and the absence of clue cells on microscopic examination.

How Supplied:

How supplied clindamycin phosphate vaginal cream 2%, is supplied as follows: 40 g tube (with 7 disposable applicators) ndc 59762-5009-1 store at controlled room temperature 20° to 25° c (68° to 77° f) [see usp]. protect from freezing.

Information for Patients:

Information for the patient the patient should be instructed not to engage in vaginal intercourse, or use other vaginal products (such as tampons or douches) during treatment with this product. the patient should also be advised that this cream contains mineral oil that may weaken latex or rubber products such as condoms or vaginal contraceptive diaphragms. therefore, use of such products within 72 hours following treatment with clindamycin phosphate vaginal cream 2%, is not recommended.

Package Label Principal Display Panel:

Principal display panel - 40 gram tube label ndc 59762-5009-1 40 gram greenstone ® brand clindamycin phosphate vaginal cream, usp 2%* rx only store at controlled room temperature 20° to 25°c (68° to 77°f) [see usp]. protect from freezing. for intravaginal use only. not for ophthalmic, dermal or oral use. avoid contact with eyes. dosage and use: see accompanying prescribing information. *each gram contains clindamycin phosphate equivalent to 20 mg (2%) of clindamycin. also contains sorbitan monostearate, polysorbate 60, propylene glycol, stearic acid, cetostearyl alcohol, mixed fatty acid esters, mineral oil, benzyl alcohol, and purified water. distributed by: greenstone llc peapack, nj 07977 lot exp paa049601 principal display panel - 40 gram tube label

Principal display panel - 40 gram tube carton ndc 59762-5009-1 40 gram with 7 applicators greenstone ® brand clindamycin phosphate vaginal cream, usp 2%* for intravaginal use only rx only principal display panel - 40 gram tube carton


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