humane acne wash
Generic: benzoly peroxide
Labeler: banner 1 llcDrug Facts
Product Profile
Brand Name
humane acne wash
Generic Name
benzoly peroxide
Labeler
banner 1 llc
Dosage Form
CREAM
Routes
Active Ingredients
benzoyl peroxide 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
69919-021
Product ID
69919-021_3f8ac133-1059-1774-e063-6294a90a3a04
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2026-12-31
Marketing Start
2015-05-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69919021
Hyphenated Format
69919-021
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
humane acne wash (source: ndc)
Generic Name
benzoly peroxide (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 1 TUBE in 1 CARTON (69919-021-01) / 237 mL in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3f8ac133-1059-1774-e063-6294a90a3a04", "openfda": {"unii": ["W9WZN9A0GM"], "rxcui": ["142034"], "spl_set_id": ["7674be57-7a8c-449e-9f48-2b772c58c88b"], "manufacturer_name": ["Banner 1 LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69919-021-01) / 237 mL in 1 TUBE", "package_ndc": "69919-021-01", "marketing_start_date": "20170208"}], "brand_name": "humane acne wash", "product_id": "69919-021_3f8ac133-1059-1774-e063-6294a90a3a04", "dosage_form": "CREAM", "product_ndc": "69919-021", "generic_name": "Benzoly Peroxide", "labeler_name": "Banner 1 LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "humane acne wash", "active_ingredients": [{"name": "BENZOYL PEROXIDE", "strength": "100 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150528", "listing_expiration_date": "20261231"}