Package 73168-004-00

Brand: uriflex fast acting analgesic pain relief

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 73168-004-00
Digits Only 7316800400
Product NDC 73168-004
Description

118 mL in 1 JAR (73168-004-00)

Marketing

Marketing Status
Marketed Since 2019-05-20
Brand uriflex fast acting analgesic pain relief
Generic menthol
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "09751fc7-6657-c196-e063-6294a90a4a57", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["2171392"], "spl_set_id": ["fb78f705-b838-461d-b42c-8c98d3ca5d09"], "manufacturer_name": ["Rejuvica LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 JAR (73168-004-00)", "package_ndc": "73168-004-00", "marketing_start_date": "20190520"}], "brand_name": "URIFLEX Fast Acting Analgesic Pain Relief", "product_id": "73168-004_09751fc7-6657-c196-e063-6294a90a4a57", "dosage_form": "CREAM", "product_ndc": "73168-004", "generic_name": "MENTHOL", "labeler_name": "Rejuvica LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "URIFLEX Fast Acting Analgesic Pain Relief", "active_ingredients": [{"name": "MENTHOL", "strength": "45 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190520", "listing_expiration_date": "20261231"}