atrix acne treatment
Generic: salicylic acid
Labeler: puretek corporationDrug Facts
Product Profile
Brand Name
atrix acne treatment
Generic Name
salicylic acid
Labeler
puretek corporation
Dosage Form
CREAM
Routes
Active Ingredients
salicylic acid 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
59088-446
Product ID
59088-446_23729830-1c13-b7f0-e063-6394a90ac4d3
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2026-12-31
Marketing Start
2021-04-06
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59088446
Hyphenated Format
59088-446
Supplemental Identifiers
RxCUI
UPC
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
atrix acne treatment (source: ndc)
Generic Name
salicylic acid (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 59 mL in 1 TUBE (59088-446-05)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "23729830-1c13-b7f0-e063-6394a90ac4d3", "openfda": {"upc": ["0359088446058"], "unii": ["O414PZ4LPZ"], "rxcui": ["317152"], "spl_set_id": ["ba106b20-32aa-df90-e053-2995a90adaef"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 TUBE (59088-446-05)", "package_ndc": "59088-446-05", "marketing_start_date": "20210406"}], "brand_name": "Atrix Acne Treatment", "product_id": "59088-446_23729830-1c13-b7f0-e063-6394a90ac4d3", "dosage_form": "CREAM", "product_ndc": "59088-446", "generic_name": "Salicylic Acid", "labeler_name": "PureTek Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Atrix Acne Treatment", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "20 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210406", "listing_expiration_date": "20261231"}