asperflex original maximum strength

Generic: menthol

Labeler: akron pharma inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name asperflex original maximum strength
Generic Name menthol
Labeler akron pharma inc.
Dosage Form PATCH
Routes
TOPICAL
Active Ingredients

menthol 210 mg/1

Manufacturer
Akron Pharma Inc.

Identifiers & Regulatory

Product NDC 71399-4461
Product ID 71399-4461_40333bee-748e-0b43-e063-6394a90a149c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2021-11-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713994461
Hyphenated Format 71399-4461

Supplemental Identifiers

RxCUI
1010823
UPC
0371399446152
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 asperflex original maximum strength (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 210 mg/1
source: ndc
Packaging
  • 5 PATCH in 1 CARTON (71399-4461-5) / 1 PATCH in 1 PATCH
source: ndc

Packages (1)

Ingredients (1)

menthol (210 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "40333bee-748e-0b43-e063-6394a90a149c", "openfda": {"upc": ["0371399446152"], "unii": ["L7T10EIP3A"], "rxcui": ["1010823"], "spl_set_id": ["d766c61e-c48b-4aff-97b0-678159479e03"], "manufacturer_name": ["Akron Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 PATCH in 1 CARTON (71399-4461-5)  / 1 PATCH in 1 PATCH", "package_ndc": "71399-4461-5", "marketing_start_date": "20211104"}], "brand_name": "AsperFlex Original Maximum Strength", "product_id": "71399-4461_40333bee-748e-0b43-e063-6394a90a149c", "dosage_form": "PATCH", "product_ndc": "71399-4461", "generic_name": "Menthol", "labeler_name": "Akron Pharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AsperFlex Original Maximum Strength", "active_ingredients": [{"name": "MENTHOL", "strength": "210 mg/1"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211104", "listing_expiration_date": "20261231"}