proski benzo

Generic: benzoyl peroxide

Labeler: pharmamed usa inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name proski benzo
Generic Name benzoyl peroxide
Labeler pharmamed usa inc
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

benzoyl peroxide 5 g/100g

Manufacturer
PHARMAMED USA INC

Identifiers & Regulatory

Product NDC 84289-216
Product ID 84289-216_30a66a1c-0afc-8695-e063-6294a90ab355
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M006
Listing Expiration 2026-12-31
Marketing Start 2025-04-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84289216
Hyphenated Format 84289-216

Supplemental Identifiers

RxCUI
308694
UNII
W9WZN9A0GM

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name proski benzo (source: ndc)
Generic Name benzoyl peroxide (source: ndc)
Application Number M006 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 5 g/100g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (84289-216-20) / 20 g in 1 TUBE
source: ndc

Packages (1)

84289-216-20 1 TUBE in 1 CARTON (84289-216-20) / 20 g in 1 TUBE

Ingredients (1)

benzoyl peroxide (5 g/100g)

Linked Drug Pages (1)

PROSKI BENZO ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "30a66a1c-0afc-8695-e063-6294a90ab355", "openfda": {"unii": ["W9WZN9A0GM"], "rxcui": ["308694"], "spl_set_id": ["2c75b3b9-6321-dede-e063-6394a90a5880"], "manufacturer_name": ["PHARMAMED USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (84289-216-20)  / 20 g in 1 TUBE", "package_ndc": "84289-216-20", "marketing_start_date": "20250401"}], "brand_name": "PROSKI BENZO", "product_id": "84289-216_30a66a1c-0afc-8695-e063-6294a90ab355", "dosage_form": "GEL", "product_ndc": "84289-216", "generic_name": "BENZOYL PEROXIDE", "labeler_name": "PHARMAMED USA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PROSKI BENZO", "active_ingredients": [{"name": "BENZOYL PEROXIDE", "strength": "5 g/100g"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}