acne control cleanser
Generic: salicylic acid
Labeler: walmart inc.Drug Facts
Product Profile
Brand Name
acne control cleanser
Generic Name
salicylic acid
Labeler
walmart inc.
Dosage Form
LIQUID
Routes
Active Ingredients
salicylic acid 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
79903-339
Product ID
79903-339_4bd4d7a6-f982-a821-e063-6294a90a8e77
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2027-12-31
Marketing Start
2025-05-16
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
79903339
Hyphenated Format
79903-339
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
acne control cleanser (source: ndc)
Generic Name
salicylic acid (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 355 mL in 1 BOTTLE, PLASTIC (79903-339-12)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4bd4d7a6-f982-a821-e063-6294a90a8e77", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["562600"], "spl_set_id": ["2df52d35-dbb6-1d35-e063-6394a90ae110"], "manufacturer_name": ["Walmart Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE, PLASTIC (79903-339-12)", "package_ndc": "79903-339-12", "marketing_start_date": "20250516"}], "brand_name": "Acne Control Cleanser", "product_id": "79903-339_4bd4d7a6-f982-a821-e063-6294a90a8e77", "dosage_form": "LIQUID", "product_ndc": "79903-339", "generic_name": "Salicylic acid", "labeler_name": "Walmart Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acne Control Cleanser", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "20 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250516", "listing_expiration_date": "20271231"}