benova pain and itch relief
Generic: menthol, 0.11%
Labeler: benova rx llcDrug Facts
Product Profile
Brand Name
benova pain and itch relief
Generic Name
menthol, 0.11%
Labeler
benova rx llc
Dosage Form
LOTION
Routes
Active Ingredients
menthol 1.1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
87150-001
Product ID
87150-001_42513ee2-8b41-a9f3-e063-6394a90a9386
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2025-12-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
87150001
Hyphenated Format
87150-001
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
benova pain and itch relief (source: ndc)
Generic Name
menthol, 0.11% (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.1 mg/mL
Packaging
- 90 mL in 1 BOTTLE, WITH APPLICATOR (87150-001-03)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}