Package 87150-001-03

Brand: benova pain and itch relief

Generic: menthol, 0.11%
NDC Package

Package Facts

Identity

Package NDC 87150-001-03
Digits Only 8715000103
Product NDC 87150-001
Product ID 87150-001_42513ee2-8b41-a9f3-e063-6394a90a9386
Description

90 mL in 1 BOTTLE, WITH APPLICATOR (87150-001-03)

Marketing

Marketing Status
Marketed Since 2025-12-15
Brand benova pain and itch relief
Generic menthol, 0.11%
Sample Package No

Linked Drug Pages (1)

BENOVA PAIN AND ITCH RELIEF ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "42513ee2-8b41-a9f3-e063-6394a90a9386", "openfda": {"upc": ["0860008040763"], "unii": ["L7T10EIP3A"], "rxcui": ["2728901"], "spl_set_id": ["42513ee2-8b40-a9f3-e063-6394a90a9386"], "manufacturer_name": ["BENOVA RX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 mL in 1 BOTTLE, WITH APPLICATOR (87150-001-03)", "package_ndc": "87150-001-03", "marketing_start_date": "20251215"}], "brand_name": "BENOVA PAIN AND ITCH RELIEF", "product_id": "87150-001_42513ee2-8b41-a9f3-e063-6394a90a9386", "dosage_form": "LOTION", "product_ndc": "87150-001", "generic_name": "MENTHOL, 0.11%", "labeler_name": "BENOVA RX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BENOVA PAIN AND ITCH RELIEF", "active_ingredients": [{"name": "MENTHOL", "strength": "1.1 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251215", "listing_expiration_date": "20261231"}