Benzamycin

Erythromycin And Benzoyl Peroxide


Bausch Health Us, Llc
Human Prescription Drug
NDC 0187-5205
Benzamycin also known as Erythromycin And Benzoyl Peroxide is a human prescription drug labeled by 'Bausch Health Us, Llc'. National Drug Code (NDC) number for Benzamycin is 0187-5205. This drug is available in dosage form of Kit. The names of the active, medicinal ingredients in Benzamycin drug includes . The currest status of Benzamycin drug is Active.

Drug Information:

Drug NDC: 0187-5205
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: Benzamycin
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: Erythromycin And Benzoyl Peroxide
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: Kit
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:
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:
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: 26 Oct, 1984
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 31 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: NDA050557
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:213082
244374
308694
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:
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.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
0187-5205-461 KIT in 1 BOX (0187-5205-46) * 1.6 g in 1 VIAL, PLASTIC * 40 g in 1 JAR26 Oct, 1984N/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:

Benzamycin erythromycin and benzoyl peroxide erythromycin erythromycin erythromycin erythromycin benzoyl peroxide benzoyl peroxide benzoyl peroxide benzoyl peroxide water carbomer homopolymer type c (allyl pentaerythritol crosslinked) alcohol sodium hydroxide docusate sodium

Indications and Usage:

Indications and usage benzamycin topical gel is indicated for the topical treatment of acne vulgaris.

Warnings:

Warnings pseudomembranous colitis has been reported with nearly all antibacterial agents, including erythromycin, and may range in severity from mild to life-threatening. therefore, it is important to consider this diagnosis in patients who present with diarrhea subsequent to the administration of antibacterial agents. treatment with antibacterial agents alters the normal flora of the colon and may permit overgrowth of clostridia. studies indicate that a toxin produced by clostridium difficile is one primary cause of “antibiotic-associated colitis”. after the diagnosis of pseudomembranous colitis has been established, therapeutic measures should be initiated. mild cases of pseudomembranous colitis usually respond to drug discontinuation 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 c. difficile colitis.

General Precautions:

General: for topical use only; not for ophthalmic use. concomitant topical acne therapy should be used with caution because a possible cumulative irritancy effect may occur, especially with the use of peeling, desquamating or abrasive agents. if severe irritation develops, discontinue use and institute appropriate therapy. the use of antibiotic agents may be associated with the overgrowth of nonsusceptible organisms including fungi. if this occurs, discontinue use and take appropriate measures. avoid contact with eyes and all mucous membranes.

Dosage and Administration:

Dosage and administration benzamycin topical gel should be applied twice daily, morning and evening, or as directed by a physician, to affected areas after the skin is thoroughly washed, rinsed with warm water and gently patted dry.

Contraindications:

Contraindications benzamycin topical gel is contraindicated in those individuals who have shown hypersensitivity to any of its components.

Adverse Reactions:

Adverse reactions in controlled clinical trials, the incidence of adverse reactions associated with the use of benzamycin topical gel was approximately 3%. these were dryness and urticarial reaction. the following additional local adverse reactions have been reported occasionally: irritation of the skin including peeling, itching, burning sensation, erythema, inflammation of the face, eyes and nose, and irritation of the eyes. skin discoloration, oiliness and tenderness of the skin have also been reported. 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.

Use in Pregnancy:

Pregnancy: teratogenic effects: animal reproduction studies have not been conducted with benzamycin topical gel or benzoyl peroxide. there was no evidence of teratogenicity or any other adverse effect on reproduction in female rats fed erythromycin base (up to 0.25% diet) prior to and during mating, during gestation and through weaning of two successive litters. there are no well-controlled trials in pregnant women with benzamycin topical gel. it also is not known whether benzamycin topical gel can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. benzamycin topical gel should be given to a pregnant woman only if clearly needed.

Pediatric Use:

Pediatric use: safety and effectiveness of this product in pediatric patients below the age of 12 have not been established.

Description:

Description benzamycin ® topical gel contains erythromycin [(3r*,4s*,5s*,6r*, 7r*, 9r*, 11r*, 12r*, 13s*, 14r*)-4-[(2,6-dideoxy-3- c -methyl-3- o -methyl-α-l- ribo -hexopyranosyl)-oxy]-14-ethyl-7,12,13-trihydroxy-3,5,7,9,11,13-hexamethyl-6-[[3,4,6-trideoxy-3-(dimethylamino)-β-d- xylo -hexopyranosyl]oxy]oxacyclotetradecane-2,10-dione]. erythromycin is a macrolide antibiotic produced from a strain of saccharopolyspora erythraea (formerly streptomyces erythreus ). it is a base and readily forms salts with acids. chemically erythromycin is c 37 h 67 no 13 . it has the following structural formula: erythromycin has the molecular weight of 733.94. it is a white crystalline powder and has a solubility of approximately 1 mg/ml in water and is soluble in alcohol at 25°c. benzamycin topical gel also contains benzoyl peroxide for topical use. benzoyl peroxide is an antibacterial and keratolytic agent. chemically benzoyl peroxide is c 14 h 10 o 4 . it has the following structural formula: benzoyl peroxide has the molecular weight of 242.23. it is a white granular powder and is sparingly soluble in water and alcohol and soluble in acetone, chloroform and ether. each gram of benzamycin topical gel contains, as dispensed, 30 mg (3%) of erythromycin and 50 mg (5%) of benzoyl peroxide in a base of purified water usp, carbomer homopolymer type c, alcohol 20%, sodium hydroxide nf, docusate sodium and fragrance. chemstructure.jpg structuralform.jpg

Clinical Pharmacology:

Clinical pharmacology the exact mechanism by which erythromycin reduces lesions of acne vulgaris is not fully known; however, the effect appears to be due in part to the antibacterial activity of the drug. benzoyl peroxide has a keratolytic and desquamative effect which may also contribute to its efficacy. benzoyl peroxide has been shown to be absorbed by the skin where it is converted to benzoic acid.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility data from a study using mice known to be highly susceptible to cancer suggests that benzoyl peroxide acts as a tumor promoter. the clinical significance of this is unknown. no animal studies have been performed to evaluate the carcinogenic and mutagenic potential or effects on fertility of topical erythromycin. however, long-term (2-year) oral studies in rats with erythromycin ethylsuccinate and erythromycin base did not provide evidence of tumorigenicity. there was no apparent effect on male or female fertility in rats fed erythromycin (base) at levels up to 0.25% of diet.

How Supplied:

How supplied and compounding directions: size benzoyl peroxide gel active erythromycin powder (in plastic vial) 70% ethyl alcohol to be added (net weight) ndc 46.6 grams 0187-5205-46 40 grams 1.6 grams 6 ml (as dispensed) prior to dispensing, tap vial until all powder flows freely. add indicated amount of room temperature 70% ethyl alcohol to vial (to the mark) and immediately shake to completely dissolve erythromycin. add this solution to gel and stir until homogeneous in appearance (1 to 1½ minutes). benzamycin topical gel should then be stored under refrigeration. do not freeze. place a 3-month expiration date on the label. note: prior to reconstitution, store at room temperature between 15° to 30°c (59° to 86°f). after reconstitution, store under refrigeration between 2° to 8°c (36° to 46°f). do not freeze. keep tightly closed. keep out of reach of children.

Information for Patients:

Information for patients: patients using benzamycin topical gel should receive the following information and instructions: 1. this medication is to be used as directed by the physician. it is for external use only. avoid contact with the eyes, nose, mouth, and all mucous membranes. 2. this medication should not be used for any disorder other than that for which it was prescribed. 3. patients should not use any other topical acne preparation unless otherwise directed by their physician. 4. patients should report to their physician any signs of local adverse reactions. 5. benzamycin topical gel may bleach hair or colored fabric. 6. keep product refrigerated and discard after 3 months.

Package Label Principal Display Panel:

Principal display panel - 46.6 g jar carton ndc 0187-5205-46 rx only benzamycin ® topical gel erythromycin-benzoyl peroxide gel for topical use only one 46.6 g jar (as dispensed) ortho dermatologics cartonjar


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