Package 56104-501-00

Brand: liquid callus remover

Generic: salicylic acid
NDC Package

Package Facts

Identity

Package NDC 56104-501-00
Digits Only 5610450100
Product NDC 56104-501
Product ID 56104-501_40aba81a-36f9-82cc-e063-6394a90a3b06
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (56104-501-00) / 9.8 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2023-09-11
Brand liquid callus remover
Generic salicylic acid
Sample Package No

Linked Drug Pages (0)

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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"}