4% menthol pain relief

Generic: menthol

Labeler: universal distribution center llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name 4% menthol pain relief
Generic Name menthol
Labeler universal distribution center llc
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

menthol, unspecified form 4 g/100mL

Manufacturer
Universal Distribution Center LLC

Identifiers & Regulatory

Product NDC 52000-439
Product ID 52000-439_8beb3f46-515f-4b8d-ad05-06be2df6ca08
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2027-12-31
Marketing Start 2026-01-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52000439
Hyphenated Format 52000-439

Supplemental Identifiers

RxCUI
415974
UPC
0676979560366
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 4% menthol pain relief (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 4 g/100mL
source: ndc
Packaging
  • 74 mL in 1 BOTTLE (52000-439-25)
source: ndc

Packages (1)

Ingredients (1)

menthol, unspecified form (4 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "8beb3f46-515f-4b8d-ad05-06be2df6ca08", "openfda": {"upc": ["0676979560366"], "unii": ["L7T10EIP3A"], "rxcui": ["415974"], "spl_set_id": ["7fb95135-4151-4ef4-bb6d-75251cafff6c"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "74 mL in 1 BOTTLE (52000-439-25)", "package_ndc": "52000-439-25", "marketing_start_date": "20260119"}], "brand_name": "4% Menthol PAIN RELIEF", "product_id": "52000-439_8beb3f46-515f-4b8d-ad05-06be2df6ca08", "dosage_form": "GEL", "product_ndc": "52000-439", "generic_name": "Menthol", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "4% Menthol PAIN RELIEF", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "4 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260119", "listing_expiration_date": "20271231"}