Package 54273-009-01

Brand: zims max freeze pro formula

Generic: menthol, unspecified form
NDC Package

Package Facts

Identity

Package NDC 54273-009-01
Digits Only 5427300901
Product NDC 54273-009
Product ID 54273-009_171be518-73bb-4425-9565-1545166d3f51
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (54273-009-01) / 89 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2018-08-20
Brand zims max freeze pro formula
Generic menthol, unspecified form
Sample Package No

Linked Drug Pages (1)

ZIMS MAX FREEZE PRO FORMULA ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "171be518-73bb-4425-9565-1545166d3f51", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["866084"], "spl_set_id": ["4d91baf3-9655-4786-93b8-aa0d93fe0bf9"], "manufacturer_name": ["KOBAYASHI Healthcare International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (54273-009-01)  / 89 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "54273-009-01", "marketing_start_date": "20180820"}], "brand_name": "ZIMS MAX FREEZE PRO FORMULA", "product_id": "54273-009_171be518-73bb-4425-9565-1545166d3f51", "dosage_form": "LIQUID", "product_ndc": "54273-009", "generic_name": "MENTHOL, UNSPECIFIED FORM", "labeler_name": "KOBAYASHI Healthcare International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ZIMS MAX FREEZE", "brand_name_suffix": "PRO FORMULA", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "160 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180820", "listing_expiration_date": "20261231"}