pain relief

Generic: menthol

Labeler: pain relieving spray inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief
Generic Name menthol
Labeler pain relieving spray inc.
Dosage Form AEROSOL, SPRAY
Routes
TOPICAL
Active Ingredients

menthol 70 mg/L

Manufacturer
Pain Relieving Spray Inc.

Identifiers & Regulatory

Product NDC 84638-8201
Product ID 84638-8201_1f44466f-0450-70fe-e063-6294a90ad575
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2025-03-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 846388201
Hyphenated Format 84638-8201

Supplemental Identifiers

RxCUI
1086713
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 menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 70 mg/L
source: ndc
Packaging
  • .059 L in 1 BOTTLE, SPRAY (84638-8201-1)
source: ndc

Packages (1)

84638-8201-1 .059 L in 1 BOTTLE, SPRAY (84638-8201-1)

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": "1f44466f-0450-70fe-e063-6294a90ad575", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["1086713"], "spl_set_id": ["1f44466f-044f-70fe-e063-6294a90ad575"], "manufacturer_name": ["Pain Relieving Spray Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".059 L in 1 BOTTLE, SPRAY (84638-8201-1)", "package_ndc": "84638-8201-1", "marketing_start_date": "20250331"}], "brand_name": "Pain Relief", "product_id": "84638-8201_1f44466f-0450-70fe-e063-6294a90ad575", "dosage_form": "AEROSOL, SPRAY", "product_ndc": "84638-8201", "generic_name": "Menthol", "labeler_name": "Pain Relieving Spray Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "active_ingredients": [{"name": "MENTHOL", "strength": "70 mg/L"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250331", "listing_expiration_date": "20261231"}