liquid callus remover

Generic: salicylic acid

Labeler: premier brands of america inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name liquid callus remover
Generic Name salicylic acid
Labeler premier brands of america inc.
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

salicylic acid 170 mg/mL

Manufacturer
Premier Brands of America Inc.

Identifiers & Regulatory

Product NDC 56104-501
Product ID 56104-501_40aba81a-36f9-82cc-e063-6394a90a3b06
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M030
Listing Expiration 2026-12-31
Marketing Start 2023-09-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 56104501
Hyphenated Format 56104-501

Supplemental Identifiers

RxCUI
312881
UNII
O414PZ4LPZ

Packaging Origin

Original Packager
true

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 liquid callus remover (source: ndc)
Generic Name salicylic acid (source: ndc)
Application Number M030 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 170 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, WITH APPLICATOR in 1 CARTON (56104-501-00) / 9.8 mL in 1 BOTTLE, WITH APPLICATOR
source: ndc

Packages (1)

Ingredients (1)

salicylic acid (170 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "40aba81a-36f9-82cc-e063-6394a90a3b06", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["312881"], "spl_set_id": ["051c7917-76ea-c7f8-e063-6394a90a9e36"], "manufacturer_name": ["Premier Brands of America Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (56104-501-00)  / 9.8 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "56104-501-00", "marketing_start_date": "20230911"}], "brand_name": "Liquid Callus Remover", "product_id": "56104-501_40aba81a-36f9-82cc-e063-6394a90a3b06", "dosage_form": "LIQUID", "product_ndc": "56104-501", "generic_name": "Salicylic Acid", "labeler_name": "Premier Brands of America Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Liquid Callus Remover", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "170 mg/mL"}], "application_number": "M030", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230911", "listing_expiration_date": "20261231"}