Loprox

Ciclopirox


Bausch Health Us, Llc
Human Prescription Drug
NDC 99207-010
Loprox also known as Ciclopirox is a human prescription drug labeled by 'Bausch Health Us, Llc'. National Drug Code (NDC) number for Loprox is 99207-010. This drug is available in dosage form of Shampoo. The names of the active, medicinal ingredients in Loprox drug includes Ciclopirox - 10 mg/.96mL . The currest status of Loprox drug is Active.

Drug Information:

Drug NDC: 99207-010
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: Loprox
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: Ciclopirox
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Bausch Health Us, Llc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Shampoo
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:CICLOPIROX - 10 mg/.96mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:TOPICAL
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
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: 20 Mar, 2003
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 21 Dec, 2025
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: NDA021159
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:Bausch Health US, LLC
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:250344
544743
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.
NUI:N0000008577
N0000008841
N0000008853
N0000000150
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:19W019ZDRJ
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 MOA:Protein Synthesis Inhibitors [MoA]
Mechanism of action of the drug—molecular, subcellular, or cellular functional activity—of the drug’s established pharmacologic class. Takes the form of the mechanism of action, followed by `[MoA]` (such as `Calcium Channel Antagonists [MoA]` or `Tumor Necrosis Factor Receptor Blocking Activity [MoA]`.
Pharmacologic Class PE:Decreased DNA Replication [PE]
Decreased Protein Synthesis [PE]
Decreased RNA Replication [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class:Decreased DNA Replication [PE]
Decreased Protein Synthesis [PE]
Decreased RNA Replication [PE]
Protein Synthesis Inhibitors [MoA]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
99207-010-101 BOTTLE, PLASTIC in 1 CARTON (99207-010-10) / 120 mL in 1 BOTTLE, PLASTIC20 Mar, 2003N/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:

Loprox ciclopirox ciclopirox ciclopirox disodium laureth sulfosuccinate laureth-2 water sodium chloride sodium laureth-3 sulfate

Indications and Usage:

1 indications and usage loprox ® (ciclopirox) shampoo, 1% is indicated for the topical treatment of seborrheic dermatitis of the scalp in adults. • loprox shampoo is an antifungal indicated for the topical treatment of seborrheic dermatitis of the scalp in adults. ( 1 )

Warnings and Cautions:

5 warnings and precautions • if signs of irritation occur, discontinue use. ( 5.1 ) • avoid contact with eyes. ( 5.1 ) • hair discoloration has been reported with loprox use. ( 5.1 ) 5.1 local effects if a reaction suggesting sensitivity or irritation occurs with the use of loprox shampoo, treatment should be discontinued and appropriate therapy instituted. contact of loprox shampoo with the eyes should be avoided. if contact occurs, rinse thoroughly with water. in patients with lighter hair color, hair discoloration has been reported.

Dosage and Administration:

2 dosage and administration loprox shampoo is not for ophthalmic, oral, or intravaginal use. wet hair and apply approximately 1 teaspoon (5 ml) of loprox shampoo to the scalp. up to 2 teaspoons (10 ml) may be used for long hair. lather and leave on hair and scalp for 3 minutes. a timer may be used. avoid contact with eyes. rinse off. treatment should be repeated twice per week for 4 weeks, with a minimum of 3 days between applications. if a patient with seborrheic dermatitis shows no clinical improvement after 4 weeks of treatment with loprox shampoo, the diagnosis should be reviewed. • apply approximately 1 teaspoon of loprox shampoo to the scalp twice per week for 4 weeks. ( 2 ) • for topical use only. not for ophthalmic, oral, or intravaginal use. ( 2 )

Dosage Forms and Strength:

3 dosage forms and strengths loprox is a shampoo containing 1% ciclopirox. each gram (equivalent to 0.96 ml) of loprox shampoo contains 10 mg ciclopirox in a colorless and translucent shampoo base. • shampoo, 1% ( 3 )

Contraindications:

4 contraindications none. none ( 4 )

Adverse Reactions:

6 adverse reactions • the most frequently reported adverse reactions are pruritus, burning, and erythema. ( 6.1 ) to report suspected adverse reactions, contact bausch health us, llc at 1-800-321-4576 or fda at 1-800-fda-1088 or www.fda.gov/medwatch. 6.1 clinical trials experience because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice. in 626 subjects treated with loprox shampoo twice weekly in the two pivotal clinical trials, the most frequent adverse events were increased itching in 1% of subjects, and application site reactions, such as burning, erythema, and itching, also in 1% of subjects. 6.2 postmarketing experience the following adverse reactions have been identified during post-approval use of loprox shampoo: hair discoloration and abnormal hair texture, alop
ecia, irritation, and rash. because these events are reported voluntarily from a population of uncertain size, it is not possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Use in Specific Population:

8 use in specific populations 8.1 pregnancy teratogenic effects: pregnancy category b there are no adequate or well-controlled studies in pregnant women. therefore, loprox shampoo should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. oral embryofetal developmental studies were conducted in mice, rats, rabbits, and monkeys. ciclopirox or ciclopirox olamine was orally administered during the period of organogenesis. no maternal toxicity, embryotoxicity or teratogenicity were noted at the highest doses of 77, 125, 80, and 38.5 mg/kg/day ciclopirox in mice, rats, rabbits, and monkeys, respectively (approximately 13, 42, 54, and 26 times the maximum recommended human dose based on body surface area comparisons, respectively). dermal embryofetal developmental studies were conducted in rats and rabbits with ciclopirox olamine dissolved in peg 400. ciclopirox olamine was topically administered during the period of organogenesis. no maternal to
xicity, embryotoxicity, or teratogenicity were noted at the highest doses of 92 mg/kg/day and 77 mg/kg/day ciclopirox in rats and rabbits, respectively (approximately 31 and 54 times the maximum recommended human dose based on body surface area comparisons, respectively). 8.3 nursing mothers it is not known whether this drug is excreted in human milk. because many drugs are excreted in human milk, caution should be exercised when loprox shampoo is administered to a nursing woman. 8.4 pediatric use no clinical trials have been conducted in subjects younger than 16 years. 8.5 geriatric use in clinical trials, the safety and tolerability of loprox shampoo in the population 65 years and older was comparable to that of younger subjects. results of the efficacy analysis in those subjects 65 years and older showed effectiveness in 25 of 85 (29%) subjects treated with loprox shampoo, and in 15 of 61 (25%) subjects treated with the vehicle; due to the small sample size, a statistically significant difference was not demonstrated. other reported clinical experience has not identified differences in responses between the elderly and younger subjects, but greater sensitivity to adverse effects in some older individuals cannot be ruled out.

Use in Pregnancy:

8.1 pregnancy teratogenic effects: pregnancy category b there are no adequate or well-controlled studies in pregnant women. therefore, loprox shampoo should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. oral embryofetal developmental studies were conducted in mice, rats, rabbits, and monkeys. ciclopirox or ciclopirox olamine was orally administered during the period of organogenesis. no maternal toxicity, embryotoxicity or teratogenicity were noted at the highest doses of 77, 125, 80, and 38.5 mg/kg/day ciclopirox in mice, rats, rabbits, and monkeys, respectively (approximately 13, 42, 54, and 26 times the maximum recommended human dose based on body surface area comparisons, respectively). dermal embryofetal developmental studies were conducted in rats and rabbits with ciclopirox olamine dissolved in peg 400. ciclopirox olamine was topically administered during the period of organogenesis. no maternal toxicity, embryotoxicity, or ter
atogenicity were noted at the highest doses of 92 mg/kg/day and 77 mg/kg/day ciclopirox in rats and rabbits, respectively (approximately 31 and 54 times the maximum recommended human dose based on body surface area comparisons, respectively).

Pediatric Use:

8.4 pediatric use no clinical trials have been conducted in subjects younger than 16 years.

Geriatric Use:

8.5 geriatric use in clinical trials, the safety and tolerability of loprox shampoo in the population 65 years and older was comparable to that of younger subjects. results of the efficacy analysis in those subjects 65 years and older showed effectiveness in 25 of 85 (29%) subjects treated with loprox shampoo, and in 15 of 61 (25%) subjects treated with the vehicle; due to the small sample size, a statistically significant difference was not demonstrated. other reported clinical experience has not identified differences in responses between the elderly and younger subjects, but greater sensitivity to adverse effects in some older individuals cannot be ruled out.

Description:

11 description loprox (ciclopirox) shampoo, 1% contains the synthetic antifungal agent ciclopirox for topical use. each gram (equivalent to 0.96 ml) of loprox shampoo contains 10 mg ciclopirox in a shampoo base consisting of disodium laureth sulfosuccinate, laureth-2, purified water, sodium chloride, and sodium laureth sulfate. loprox shampoo is a colorless, translucent solution. the chemical name for ciclopirox is 6-cyclohexyl-1-hydroxy-4-methyl-2(1 h )-pyridone, with the empirical formula c 12 h 17 no 2 and a molecular weight of 207.27. the cas registry number is [29342-05-0]. the chemical structure is: loprox-01.jpg

Clinical Pharmacology:

12 clinical pharmacology 12.1 mechanism of action ciclopirox is a hydroxypyridone antifungal agent although the relevance of this property for the indication of seborrheic dermatitis is not known. ciclopirox acts by chelation of polyvalent cations (fe 3+ or al 3+ ), resulting in the inhibition of the metal-dependent enzymes that are responsible for the degradation of peroxides within the fungal cell. 12.2 pharmacodynamics the pharmacodynamics of loprox shampoo are unknown. 12.3 pharmacokinetics in a study in patients with seborrheic dermatitis of the scalp, application of 5 ml ciclopirox shampoo, 1% twice weekly for 4 weeks, with an exposure time of 3 minutes per application, resulted in detectable serum concentrations of ciclopirox in 6 out of 18 patients. the serum concentrations measured throughout the dosing interval on days 1 and 29 ranged from 10.3 ng/ml to 13.2 ng/ml. total urinary excretion of ciclopirox was less than 0.5% of the administered dose. 12.4 microbiology ciclopirox
is fungicidal in vitro against malassezia furfur ( pityrosporum spp.), p. ovale , and p. orbiculare . the clinical significance of antifungal activity in the treatment of seborrheic dermatitis is not known.

Mechanism of Action:

12.1 mechanism of action ciclopirox is a hydroxypyridone antifungal agent although the relevance of this property for the indication of seborrheic dermatitis is not known. ciclopirox acts by chelation of polyvalent cations (fe 3+ or al 3+ ), resulting in the inhibition of the metal-dependent enzymes that are responsible for the degradation of peroxides within the fungal cell.

Pharmacodynamics:

12.2 pharmacodynamics the pharmacodynamics of loprox shampoo are unknown.

Pharmacokinetics:

12.3 pharmacokinetics in a study in patients with seborrheic dermatitis of the scalp, application of 5 ml ciclopirox shampoo, 1% twice weekly for 4 weeks, with an exposure time of 3 minutes per application, resulted in detectable serum concentrations of ciclopirox in 6 out of 18 patients. the serum concentrations measured throughout the dosing interval on days 1 and 29 ranged from 10.3 ng/ml to 13.2 ng/ml. total urinary excretion of ciclopirox was less than 0.5% of the administered dose.

Nonclinical Toxicology:

13 nonclinical toxicology 13.1 carcinogenesis, mutagenesis, impairment of fertility a 104-week dermal carcinogenicity study in mice was conducted with ciclopirox cream applied at doses up to 1.93% (100 mg/kg/day or 300 mg/m 2 /day). no increase in drug-related neoplasms was noted when compared to control. the following in vitro genotoxicity tests have been conducted with ciclopirox: evaluation of gene mutation in the ames salmonella and e. coli assays (negative); chromosome aberration assays in v79 chinese hamster lung fibroblast cells, with and without metabolic activation (positive); chromosome aberration assays in v79 chinese hamster lung fibroblast cells in the presence of supplemental fe 3+ , with and without metabolic activation (negative); gene mutation assays in the hgprt-test with v79 chinese hamster lung fibroblast cells (negative); and a primary dna damage assay (i.e., unscheduled dna synthesis assay in a549 human cells) (negative). an in vitro cell transformation assay in b
alb/c 3t3 cells was negative for cell transformation. in an in vivo chinese hamster bone marrow cytogenetic assay, ciclopirox was negative for chromosome aberrations at a dosage of 5,000 mg/kg body weight. a combined oral fertility and embryofetal developmental study was conducted in rats with ciclopirox olamine. no effect on fertility or reproductive performance was noted at the highest dose tested of 3.85 mg/kg/day ciclopirox (approximately 1.3 times the maximum recommended human dose based on body surface area comparisons).

Carcinogenesis and Mutagenesis and Impairment of Fertility:

13.1 carcinogenesis, mutagenesis, impairment of fertility a 104-week dermal carcinogenicity study in mice was conducted with ciclopirox cream applied at doses up to 1.93% (100 mg/kg/day or 300 mg/m 2 /day). no increase in drug-related neoplasms was noted when compared to control. the following in vitro genotoxicity tests have been conducted with ciclopirox: evaluation of gene mutation in the ames salmonella and e. coli assays (negative); chromosome aberration assays in v79 chinese hamster lung fibroblast cells, with and without metabolic activation (positive); chromosome aberration assays in v79 chinese hamster lung fibroblast cells in the presence of supplemental fe 3+ , with and without metabolic activation (negative); gene mutation assays in the hgprt-test with v79 chinese hamster lung fibroblast cells (negative); and a primary dna damage assay (i.e., unscheduled dna synthesis assay in a549 human cells) (negative). an in vitro cell transformation assay in balb/c 3t3 cells was negati
ve for cell transformation. in an in vivo chinese hamster bone marrow cytogenetic assay, ciclopirox was negative for chromosome aberrations at a dosage of 5,000 mg/kg body weight. a combined oral fertility and embryofetal developmental study was conducted in rats with ciclopirox olamine. no effect on fertility or reproductive performance was noted at the highest dose tested of 3.85 mg/kg/day ciclopirox (approximately 1.3 times the maximum recommended human dose based on body surface area comparisons).

Clinical Studies:

14 clinical studies in two randomized, double-blind clinical trials, subjects 16 years and older with seborrheic dermatitis of the scalp applied loprox shampoo or its vehicle twice weekly for 4 weeks. subjects who were immunocompromised, those with psoriasis or atopic dermatitis, women of childbearing potential not using adequate contraception, and pregnant or lactating women were excluded from the clinical trials. an evaluation of the overall status of the seborrheic dermatitis, the presence and severity of erythema or inflammation, and scaling was made at week 4, using a scale of 0=none, 1=slight, 2=mild, 3=moderate, 4=pronounced, and 5=severe. effective treatment was defined as achieving a score of 0 (or a score of 1 if the baseline score was ≥3) simultaneously for status of the seborrheic dermatitis, erythema or inflammation, and scaling at week 4. ciclopirox shampoo was shown to be statistically significantly more effective than vehicle in both trials. efficacy results for th
e two trials are presented in table 1 below. table 1. effective treatment rates at week 4 in trials 1 and 2 ciclopirox shampoo vehicle study 1 220/380 (58%) 60/192 (31%) study 2 65/250 (26%) 32/249 (13%) efficacy for african american subjects was not demonstrated, although only 53 african american subjects were enrolled in the two pivotal trials.

How Supplied:

16 how supplied/storage and handling loprox (ciclopirox) shampoo, 1% is colorless and translucent, and supplied in 120 ml plastic bottles (ndc 99207-010-10). discard unused product after initial treatment duration. store between 15° to 30°c (59° to 86°f). keep out of reach of children.

Information for Patients:

17 patient counseling information advise the patient to read the fda-approved patient labeling ( patient information ). the patient should be instructed to: • use loprox shampoo as directed by the physician. avoid contact with the eyes. if contact occurs, rinse thoroughly with water. loprox shampoo is for external use on the scalp only. do not swallow. • use loprox shampoo for seborrheic dermatitis for the full treatment time even though symptoms may have improved. notify the physician if there is no improvement after 4 weeks. • inform the physician if the area of application shows signs of increased irritation (redness, itching, burning, blistering, swelling, or oozing). manufactured for: bausch health us, llc bridgewater, nj 08807 usa manufactured by: bausch health companies inc. laval, quebec h7l 4a8, canada loprox is a trademark of bausch health companies inc. or its affiliates. © 2019 bausch health companies inc. or its affiliates 9505303

Spl Patient Package Insert:

Patient information loprox ® (loh-proks) (ciclopirox) shampoo important: for use on the scalp only. do not get loprox shampoo in your eyes, mouth, or vagina. what is loprox shampoo? loprox shampoo is a prescription medicine used on the scalp to treat adults with a skin condition called seborrheic dermatitis. it is not known if loprox shampoo is safe and effective in children under 16 years of age. what should i tell my doctor before using loprox shampoo? before using loprox shampoo, tell your doctor if you: • have any other medical conditions. • are pregnant or plan to become pregnant. it is not known if loprox shampoo will harm your unborn baby. • are breastfeeding or plan to breastfeed. it is not known if loprox shampoo passes into your breast milk. • are taking prescription and nonprescription medicines, vitamins, and herbal supplements. know the medicines you take. keep a list of them to show your doctor and pharmacist when you get a new medicine. how should
i use loprox shampoo? • use loprox shampoo exactly as your doctor tells you to use it. • wash your hair using loprox shampoo 2 times each week for 4 weeks. there should be at least 3 days between each time you use loprox shampoo. • use loprox shampoo for 4 weeks even if your skin condition improves. • tell your doctor if your scalp condition is not getting better after you have used loprox shampoo for 4 weeks. • do not swallow loprox shampoo. • avoid getting loprox shampoo in your eyes. if loprox shampoo gets into your eyes, rinse them well with water. how should i apply loprox shampoo? • wet your hair and apply approximately 1 teaspoon of loprox shampoo to your scalp. you may use up to 2 teaspoons of loprox shampoo if you have long hair. lather and leave loprox shampoo on your hair and scalp for 3 minutes. you may use a timer. • after 3 minutes have passed, rinse your hair and scalp. what are the possible side effects of loprox shampoo? the most common side effects of loprox shampoo include: itching, burning, and redness of the scalp. tell your doctor if you get any of these symptoms and they become worse or do not go away, or if you get blistering, swelling, or oozing in your scalp. these are not all the possible side effects of loprox shampoo. for more information, ask your doctor. call your doctor for medical advice about side effects. you may report side effects to fda at 1-800-fda-1088. how should i store loprox shampoo? • store loprox shampoo at room temperature, between 59° to 86°f (15° to 30°c). • safely throw away any unused loprox shampoo after you finish your treatment. keep loprox shampoo and all medicines out of reach of children. general information about loprox shampoo medicines are sometimes prescribed for purposes other than those listed in a patient information leaflet. do not use loprox shampoo for a condition for which it was not prescribed. do not give loprox shampoo to other people, even if they have the same symptoms you have. it may harm them. you can ask your pharmacist or doctor for information about loprox shampoo that is written for health professionals. for more information about loprox shampoo, call 1-800-321-4576. what are the ingredients in loprox shampoo? active ingredient: ciclopirox inactive ingredients: disodium laureth sulfosuccinate, laureth-2, purified water, sodium chloride, and sodium laureth sulfate. this patient information has been approved by the u.s. food and drug administration. manufactured for: bausch health us, llc bridgewater, nj 08807 usa manufactured by: bausch health companies inc. laval, quebec h7l 4a8, canada loprox is a trademark of bausch health companies inc. or its affiliates. © 2019 bausch health companies inc. or its affiliates 9505303 rev. 05/2019

Package Label Principal Display Panel:

Principal display panel - 120 ml bottle carton ndc 99207-010-10 rx only loprox ® shampoo (ciclopirox) 1% for topical use only not for ophthalmic, oral or intravaginal use keep out of reach of children 120 ml ortho dermatologics carton.jpg


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