Package 73287-023-01

Brand: ultra strength pain relief gel

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 73287-023-01
Digits Only 7328702301
Product NDC 73287-023
Description

1 APPLICATOR in 1 CARTON (73287-023-01) / 71 g in 1 APPLICATOR

Marketing

Marketing Status
Marketed Since 2022-02-28
Brand ultra strength pain relief gel
Generic menthol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "275b89dc-566d-3bc1-e063-6394a90a9cad", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["d91b2e09-550e-4968-e053-2995a90ae323"], "manufacturer_name": ["TELEBRANDS CORP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 APPLICATOR in 1 CARTON (73287-023-01)  / 71 g in 1 APPLICATOR", "package_ndc": "73287-023-01", "marketing_start_date": "20220228"}], "brand_name": "Ultra Strength Pain Relief Gel", "product_id": "73287-023_275b89dc-566d-3bc1-e063-6394a90a9cad", "dosage_form": "LOTION", "product_ndc": "73287-023", "generic_name": "Menthol", "labeler_name": "TELEBRANDS CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ultra Strength Pain Relief Gel", "active_ingredients": [{"name": "MENTHOL", "strength": "8 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220228", "listing_expiration_date": "20261231"}