Package 72937-632-03

Brand: menthol

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 72937-632-03
Digits Only 7293763203
Product NDC 72937-632
Product ID 72937-632_45c5ca7e-20df-92db-e063-6294a90ac402
Description

90 mL in 1 BOTTLE, WITH APPLICATOR (72937-632-03)

Marketing

Marketing Status
Marketed Since 2025-12-20
Brand menthol
Generic menthol
Sample Package No

Linked Drug Pages (1)

MENTHOL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "45c5ca7e-20df-92db-e063-6294a90ac402", "openfda": {"upc": ["0875292791727"], "unii": ["L7T10EIP3A"], "spl_set_id": ["45c5ca6f-d425-6cfb-e063-6394a90a1b66"], "manufacturer_name": ["SUNSET PAIN RELIEF"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 mL in 1 BOTTLE, WITH APPLICATOR (72937-632-03)", "package_ndc": "72937-632-03", "marketing_start_date": "20251220"}], "brand_name": "MENTHOL", "product_id": "72937-632_45c5ca7e-20df-92db-e063-6294a90ac402", "dosage_form": "GEL", "product_ndc": "72937-632", "generic_name": "MENTHOL", "labeler_name": "SUNSET PAIN RELIEF", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MENTHOL", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "4 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251220", "listing_expiration_date": "20261231"}