Package 36800-019-04

Brand: salicylic acid

Generic: medicated callus removers
NDC Package

Package Facts

Identity

Package NDC 36800-019-04
Digits Only 3680001904
Product NDC 36800-019
Description

4 PATCH in 1 PACKAGE (36800-019-04)

Marketing

Marketing Status
Marketed Since 2012-01-03
Brand salicylic acid
Generic medicated callus removers
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4732c7db-b76a-b993-e063-6294a90aab3b", "openfda": {"upc": ["0036800054530"], "unii": ["O414PZ4LPZ"], "rxcui": ["240559"], "spl_set_id": ["c03e46a9-d4f0-4d1f-87f2-ac0efc414070"], "manufacturer_name": ["Topco Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 PATCH in 1 PACKAGE (36800-019-04)", "package_ndc": "36800-019-04", "marketing_start_date": "20120103"}], "brand_name": "Salicylic Acid", "product_id": "36800-019_4732c7db-b76a-b993-e063-6294a90aab3b", "dosage_form": "PATCH", "product_ndc": "36800-019", "generic_name": "Medicated Callus Removers", "labeler_name": "Topco Associates LLC", "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": "20120103", "listing_expiration_date": "20261231"}