wart remover gel
Generic: wart remover gel
Labeler: premier brands of america inc.Drug Facts
Product Profile
Brand Name
wart remover gel
Generic Name
wart remover gel
Labeler
premier brands of america inc.
Dosage Form
GEL
Routes
Active Ingredients
salicylic acid .17 g/g
Manufacturer
Identifiers & Regulatory
Product NDC
56104-237
Product ID
56104-237_32d28d8e-c7ac-2e09-e063-6294a90aee0a
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M028
Listing Expiration
2026-12-31
Marketing Start
2013-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
56104237
Hyphenated Format
56104-237
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
wart remover gel (source: ndc)
Generic Name
wart remover gel (source: ndc)
Application Number
M028 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .17 g/g
Packaging
- 7 g in 1 TUBE (56104-237-07)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "32d28d8e-c7ac-2e09-e063-6294a90aee0a", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["312880"], "spl_set_id": ["db4ba7ac-a58b-42d5-9181-da70309f1791"], "manufacturer_name": ["Premier Brands of America Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "7 g in 1 TUBE (56104-237-07)", "package_ndc": "56104-237-07", "marketing_start_date": "20130101"}], "brand_name": "Wart Remover Gel", "product_id": "56104-237_32d28d8e-c7ac-2e09-e063-6294a90aee0a", "dosage_form": "GEL", "product_ndc": "56104-237", "generic_name": "Wart Remover Gel", "labeler_name": "Premier Brands of America Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Wart Remover Gel", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": ".17 g/g"}], "application_number": "M028", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130101", "listing_expiration_date": "20261231"}