salicylic acid
Generic: extra thick callus removers
Labeler: walgreen companyDrug Facts
Product Profile
Brand Name
salicylic acid
Generic Name
extra thick callus removers
Labeler
walgreen company
Dosage Form
PATCH
Routes
Active Ingredients
salicylic acid 40 mg/41
Manufacturer
Identifiers & Regulatory
Product NDC
0363-7730
Product ID
0363-7730_48d3c094-bd68-3a8e-e063-6294a90abb3c
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M030
Listing Expiration
2027-12-31
Marketing Start
2012-08-16
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03637730
Hyphenated Format
0363-7730
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
salicylic acid (source: ndc)
Generic Name
extra thick callus removers (source: ndc)
Application Number
M030 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/41
Packaging
- 4 PATCH in 1 PACKAGE (0363-7730-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "48d3c094-bd68-3a8e-e063-6294a90abb3c", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["240559"], "spl_set_id": ["fa2e95b5-fe90-4406-b981-05bca62fd25c"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 PATCH in 1 PACKAGE (0363-7730-04)", "package_ndc": "0363-7730-04", "marketing_start_date": "20120816"}], "brand_name": "Salicylic Acid", "product_id": "0363-7730_48d3c094-bd68-3a8e-e063-6294a90abb3c", "dosage_form": "PATCH", "product_ndc": "0363-7730", "generic_name": "Extra Thick Callus Removers", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Salicylic Acid", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "40 mg/41"}], "application_number": "M030", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120816", "listing_expiration_date": "20271231"}