wellpatch cooling pain relief
Generic: menthol
Labeler: the mentholatum companyDrug Facts
Product Profile
Brand Name
wellpatch cooling pain relief
Generic Name
menthol
Labeler
the mentholatum company
Dosage Form
PATCH
Routes
Active Ingredients
menthol, unspecified form 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
10742-8125
Product ID
10742-8125_2978c10c-077e-152a-e063-6394a90af864
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2017-02-06
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
107428125
Hyphenated Format
10742-8125
Supplemental Identifiers
RxCUI
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
wellpatch cooling pain relief (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 1 PATCH in 1 POUCH (10742-8125-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2978c10c-077e-152a-e063-6394a90af864", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["420222", "1232426"], "spl_set_id": ["13565b05-ce32-444c-8765-cda23b0036fc"], "manufacturer_name": ["The Mentholatum Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 PATCH in 1 POUCH (10742-8125-1)", "package_ndc": "10742-8125-1", "marketing_start_date": "20170206"}], "brand_name": "WellPatch Cooling Pain Relief", "product_id": "10742-8125_2978c10c-077e-152a-e063-6394a90af864", "dosage_form": "PATCH", "product_ndc": "10742-8125", "generic_name": "menthol", "labeler_name": "The Mentholatum Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "WellPatch Cooling Pain Relief", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "50 mg/1"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170206", "listing_expiration_date": "20261231"}