pain relief

Generic: analgesic menthol

Labeler: unifirst first aid corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief
Generic Name analgesic menthol
Labeler unifirst first aid corporation
Dosage Form SPRAY
Routes
TOPICAL
Active Ingredients

menthol 70 mg/L

Manufacturer
Unifirst First Aid Corporation

Identifiers & Regulatory

Product NDC 47682-321
Product ID 47682-321_3e4ee639-9aef-38c5-e063-6394a90a9ad3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M015
Listing Expiration 2026-12-31
Marketing Start 2019-04-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 47682321
Hyphenated Format 47682-321

Supplemental Identifiers

UPC
0347682301774
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 pain relief (source: ndc)
Generic Name analgesic menthol (source: ndc)
Application Number M015 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 70 mg/L
source: ndc
Packaging
  • .059 L in 1 BOTTLE, SPRAY (47682-321-02)
source: ndc

Packages (1)

47682-321-02 .059 L in 1 BOTTLE, SPRAY (47682-321-02)

Ingredients (1)

menthol (70 mg/L)

Linked Drug Pages (1)

Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3e4ee639-9aef-38c5-e063-6394a90a9ad3", "openfda": {"upc": ["0347682301774"], "unii": ["L7T10EIP3A"], "spl_set_id": ["8162d22d-04c0-de07-e053-2991aa0a9975"], "manufacturer_name": ["Unifirst First Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".059 L in 1 BOTTLE, SPRAY (47682-321-02)", "package_ndc": "47682-321-02", "marketing_start_date": "20190401"}], "brand_name": "Pain Relief", "product_id": "47682-321_3e4ee639-9aef-38c5-e063-6394a90a9ad3", "dosage_form": "SPRAY", "product_ndc": "47682-321", "generic_name": "Analgesic Menthol", "labeler_name": "Unifirst First Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "active_ingredients": [{"name": "MENTHOL", "strength": "70 mg/L"}], "application_number": "M015", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}