salicylic acid
Generic: callus removers
Labeler: premier brands of america inc.Drug Facts
Product Profile
Brand Name
salicylic acid
Generic Name
callus removers
Labeler
premier brands of america inc.
Dosage Form
PATCH
Routes
Active Ingredients
salicylic acid 40 mg/41
Manufacturer
Identifiers & Regulatory
Product NDC
56104-013
Product ID
56104-013_4732daa9-5291-b246-e063-6294a90af602
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M030
Listing Expiration
2026-12-31
Marketing Start
2013-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
56104013
Hyphenated Format
56104-013
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
callus removers (source: ndc)
Application Number
M030 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/41
Packaging
- 4 PATCH in 1 PACKAGE (56104-013-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4732daa9-5291-b246-e063-6294a90af602", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["240559"], "spl_set_id": ["0b637f58-5604-454d-99ba-24115113ac3d"], "manufacturer_name": ["Premier Brands of America Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 PATCH in 1 PACKAGE (56104-013-04)", "package_ndc": "56104-013-04", "marketing_start_date": "20130101"}], "brand_name": "Salicylic acid", "product_id": "56104-013_4732daa9-5291-b246-e063-6294a90af602", "dosage_form": "PATCH", "product_ndc": "56104-013", "generic_name": "Callus Removers", "labeler_name": "Premier Brands of America Inc.", "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": "20130101", "listing_expiration_date": "20261231"}