arctic relief

Generic: menthol, unspecified form

Labeler: stratus pharmaceuticals inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name arctic relief
Generic Name menthol, unspecified form
Labeler stratus pharmaceuticals inc
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

menthol, unspecified form 3.969 g/113.4g

Manufacturer
STRATUS PHARMACEUTICALS INC

Identifiers & Regulatory

Product NDC 58980-615
Product ID 58980-615_db73c60c-1ff8-4b16-a467-6f0b8727f1d6
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2017-09-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58980615
Hyphenated Format 58980-615

Supplemental Identifiers

RxCUI
808955
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 arctic relief (source: ndc)
Generic Name menthol, unspecified form (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 3.969 g/113.4g
source: ndc
Packaging
  • 1 TUBE in 1 BOX (58980-615-40) / 113.4 g in 1 TUBE
source: ndc

Packages (1)

Ingredients (1)

menthol, unspecified form (3.969 g/113.4g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "db73c60c-1ff8-4b16-a467-6f0b8727f1d6", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["808955"], "spl_set_id": ["d27fbc17-46b7-4d52-ba29-c99b6c63144a"], "manufacturer_name": ["STRATUS PHARMACEUTICALS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (58980-615-40)  / 113.4 g in 1 TUBE", "package_ndc": "58980-615-40", "marketing_start_date": "20170915"}], "brand_name": "ARCTIC RELIEF", "product_id": "58980-615_db73c60c-1ff8-4b16-a467-6f0b8727f1d6", "dosage_form": "GEL", "product_ndc": "58980-615", "generic_name": "MENTHOL, UNSPECIFIED FORM", "labeler_name": "STRATUS PHARMACEUTICALS INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ARCTIC RELIEF", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "3.969 g/113.4g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170915", "listing_expiration_date": "20261231"}