replenix acne
Generic: benzoyl peroxide
Labeler: topiderm, inc.Drug Facts
Product Profile
Brand Name
replenix acne
Generic Name
benzoyl peroxide
Labeler
topiderm, inc.
Dosage Form
GEL
Routes
Active Ingredients
benzoyl peroxide 100 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
51326-412
Product ID
51326-412_d2182fb1-b7ad-47d2-9855-0cde7465add5
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2026-12-31
Marketing Start
1993-01-22
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51326412
Hyphenated Format
51326-412
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
replenix acne (source: ndc)
Generic Name
benzoyl peroxide (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/g
Packaging
- 57 g in 1 TUBE (51326-412-57)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "d2182fb1-b7ad-47d2-9855-0cde7465add5", "openfda": {"unii": ["W9WZN9A0GM"], "rxcui": ["486131"], "spl_set_id": ["c12f9005-a549-4447-9beb-df7126f77df1"], "manufacturer_name": ["Topiderm, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "57 g in 1 TUBE (51326-412-57)", "package_ndc": "51326-412-57", "marketing_start_date": "19930122"}], "brand_name": "Replenix Acne", "product_id": "51326-412_d2182fb1-b7ad-47d2-9855-0cde7465add5", "dosage_form": "GEL", "product_ndc": "51326-412", "generic_name": "Benzoyl Peroxide", "labeler_name": "Topiderm, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Replenix Acne", "active_ingredients": [{"name": "BENZOYL PEROXIDE", "strength": "100 mg/g"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19930122", "listing_expiration_date": "20261231"}