benova pain and itch relief

Generic: menthol, 0.11%

Labeler: benova rx llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name benova pain and itch relief
Generic Name menthol, 0.11%
Labeler benova rx llc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

menthol 1.1 mg/mL

Manufacturer
BENOVA RX LLC

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
2728901
UPC
0860008040763
UNII
L7T10EIP3A

Packaging Origin

Original Packager
true

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
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1.1 mg/mL
source: ndc
Packaging
  • 90 mL in 1 BOTTLE, WITH APPLICATOR (87150-001-03)
source: ndc

Packages (1)

Ingredients (1)

menthol (1.1 mg/mL)

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"}