Package 69678-143-03

Brand: kens pain and arthritis formula

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 69678-143-03
Digits Only 6967814303
Product NDC 69678-143
Description

88 mL in 1 BOTTLE (69678-143-03)

Marketing

Marketing Status
Marketed Since 2024-03-05
Brand kens pain and arthritis formula
Generic menthol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "c01c4dab-9263-43d7-88dd-5df72403f96c", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["35834473-3ad5-41ec-a110-e742aa7e2ee4"], "manufacturer_name": ["Eezaway Relief Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "88 mL in 1 BOTTLE (69678-143-03)", "package_ndc": "69678-143-03", "marketing_start_date": "20240305"}], "brand_name": "KENS PAIN AND ARTHRITIS FORMULA", "product_id": "69678-143_c01c4dab-9263-43d7-88dd-5df72403f96c", "dosage_form": "LIQUID", "product_ndc": "69678-143", "generic_name": "MENTHOL", "labeler_name": "Eezaway Relief Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "KENS PAIN AND ARTHRITIS FORMULA", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "2.75 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240305", "listing_expiration_date": "20261231"}