Package 72937-004-03

Brand: menthol

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 72937-004-03
Digits Only 7293700403
Product NDC 72937-004
Product ID 72937-004_44141d2a-1d91-b970-e063-6294a90a53f4
Description

90 mL in 1 BOTTLE, WITH APPLICATOR (72937-004-03)

Marketing

Marketing Status
Discontinued 2026-10-23
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": "44141d2a-1d91-b970-e063-6294a90a53f4", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["934d4638-b47b-187d-e053-2995a90ae69d"], "manufacturer_name": ["SUNSET PAIN RELIEF ROLL-ON 3OZ"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 mL in 1 BOTTLE, WITH APPLICATOR (72937-004-03)", "package_ndc": "72937-004-03", "marketing_end_date": "20261023", "marketing_start_date": "20190924"}], "brand_name": "MENTHOL", "product_id": "72937-004_44141d2a-1d91-b970-e063-6294a90a53f4", "dosage_form": "GEL", "product_ndc": "72937-004", "generic_name": "MENTHOL", "labeler_name": "SUNSET PAIN RELIEF ROLL-ON 3OZ", "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_end_date": "20261023", "marketing_start_date": "20190924"}