salicylic acid
Generic: wart removers
Labeler: premier brands of america inc.Drug Facts
Product Profile
Brand Name
salicylic acid
Generic Name
wart removers
Labeler
premier brands of america inc.
Dosage Form
PATCH
Routes
Active Ingredients
salicylic acid 40 mg/181
Manufacturer
Identifiers & Regulatory
Product NDC
56104-017
Product ID
56104-017_476e735c-4f3a-b6c4-e063-6394a90a8c2b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M028
Listing Expiration
2027-12-31
Marketing Start
2013-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
56104017
Hyphenated Format
56104-017
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
wart removers (source: ndc)
Application Number
M028 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/181
Packaging
- 18 PATCH in 1 BOX (56104-017-18)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "476e735c-4f3a-b6c4-e063-6394a90a8c2b", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["240559"], "spl_set_id": ["ec588377-e672-4960-a3ca-2286f72ef5a5"], "manufacturer_name": ["Premier Brands of America Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 PATCH in 1 BOX (56104-017-18)", "package_ndc": "56104-017-18", "marketing_start_date": "20130101"}], "brand_name": "Salicylic Acid", "product_id": "56104-017_476e735c-4f3a-b6c4-e063-6394a90a8c2b", "dosage_form": "PATCH", "product_ndc": "56104-017", "generic_name": "Wart 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/181"}], "application_number": "M028", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130101", "listing_expiration_date": "20271231"}