medline
Generic: menthol
Labeler: medline industries, lpDrug Facts
Product Profile
Brand Name
medline
Generic Name
menthol
Labeler
medline industries, lp
Dosage Form
PATCH
Routes
Active Ingredients
menthol 5 mg/100mg
Manufacturer
Identifiers & Regulatory
Product NDC
53329-972
Product ID
53329-972_387c2d55-f00b-422f-e063-6294a90a898e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2025-02-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53329972
Hyphenated Format
53329-972
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
medline (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/100mg
Packaging
- 5 POUCH in 1 BOX (53329-972-05) / 1 PATCH in 1 POUCH / 500 mg in 1 PATCH
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "387c2d55-f00b-422f-e063-6294a90a898e", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["420222"], "spl_set_id": ["0d947aa6-045e-d001-e063-6294a90a3657"], "manufacturer_name": ["Medline Industries, LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 POUCH in 1 BOX (53329-972-05) / 1 PATCH in 1 POUCH / 500 mg in 1 PATCH", "package_ndc": "53329-972-05", "marketing_start_date": "20250201"}], "brand_name": "Medline", "product_id": "53329-972_387c2d55-f00b-422f-e063-6294a90a898e", "dosage_form": "PATCH", "product_ndc": "53329-972", "generic_name": "menthol", "labeler_name": "Medline Industries, LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Medline", "active_ingredients": [{"name": "MENTHOL", "strength": "5 mg/100mg"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250201", "listing_expiration_date": "20261231"}