salicylic acid
Generic: wart remover gel
Labeler: walgreen companyDrug Facts
Product Profile
Brand Name
salicylic acid
Generic Name
wart remover gel
Labeler
walgreen company
Dosage Form
GEL
Routes
Active Ingredients
salicylic acid .17 g/7g
Manufacturer
Identifiers & Regulatory
Product NDC
0363-0219
Product ID
0363-0219_42f4cafa-14cf-06b2-e063-6394a90aa119
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M028
Listing Expiration
2026-12-31
Marketing Start
2012-08-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03630219
Hyphenated Format
0363-0219
Supplemental Identifiers
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
salicylic acid (source: ndc)
Generic Name
wart remover gel (source: ndc)
Application Number
M028 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .17 g/7g
Packaging
- 7 g in 1 TUBE (0363-0219-25)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "42f4cafa-14cf-06b2-e063-6394a90aa119", "openfda": {"upc": ["0311917147901"], "unii": ["O414PZ4LPZ"], "spl_set_id": ["9d73b428-b6a0-4b11-88b7-36c012d24e62"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "7 g in 1 TUBE (0363-0219-25)", "package_ndc": "0363-0219-25", "marketing_start_date": "20120824"}], "brand_name": "Salicylic Acid", "product_id": "0363-0219_42f4cafa-14cf-06b2-e063-6394a90aa119", "dosage_form": "GEL", "product_ndc": "0363-0219", "generic_name": "Wart Remover Gel", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Salicylic Acid", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": ".17 g/7g"}], "application_number": "M028", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120824", "listing_expiration_date": "20261231"}