k19 relief

Generic: menthol

Labeler: k19 llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name k19 relief
Generic Name menthol
Labeler k19 llc
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

menthol 12.5 mg/mL

Manufacturer
K19 LLC

Identifiers & Regulatory

Product NDC 83574-413
Product ID 83574-413_2bbc8ed1-176c-27a5-e063-6394a90a38ee
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2023-07-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83574413
Hyphenated Format 83574-413

Supplemental Identifiers

RxCUI
1606487
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 k19 relief (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/mL
source: ndc
Packaging
  • 295 mL in 1 BOTTLE, SPRAY (83574-413-00)
source: ndc

Packages (1)

83574-413-00 295 mL in 1 BOTTLE, SPRAY (83574-413-00)

Ingredients (1)

menthol (12.5 mg/mL)

Linked Drug Pages (1)

K19 RELIEF ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2bbc8ed1-176c-27a5-e063-6394a90a38ee", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["1606487"], "spl_set_id": ["e2e1ca96-1ae8-4c99-b8de-ce26754292f9"], "manufacturer_name": ["K19 LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "295 mL in 1 BOTTLE, SPRAY (83574-413-00)", "package_ndc": "83574-413-00", "marketing_start_date": "20230710"}], "brand_name": "K19 RELIEF", "product_id": "83574-413_2bbc8ed1-176c-27a5-e063-6394a90a38ee", "dosage_form": "LIQUID", "product_ndc": "83574-413", "generic_name": "MENTHOL", "labeler_name": "K19 LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "K19 RELIEF", "active_ingredients": [{"name": "MENTHOL", "strength": "12.5 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230710", "listing_expiration_date": "20261231"}