freeze it menthol

Generic: menthol

Labeler: liquidcapsule manufacturing llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name freeze it menthol
Generic Name menthol
Labeler liquidcapsule manufacturing llc
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

menthol 3.5 g/100g

Manufacturer
LiquidCapsule Manufacturing LLC

Identifiers & Regulatory

Product NDC 71726-004
Product ID 71726-004_6e80d075-fdc1-448f-9e11-7a6980359ef7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2025-06-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71726004
Hyphenated Format 71726-004

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 freeze it menthol (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 3.5 g/100g
source: ndc
Packaging
  • 113.4 g in 1 TUBE (71726-004-02)
source: ndc

Packages (1)

71726-004-02 113.4 g in 1 TUBE (71726-004-02)

Ingredients (1)

menthol (3.5 g/100g)

Linked Drug Pages (1)

FREEZE IT Menthol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "6e80d075-fdc1-448f-9e11-7a6980359ef7", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["808955"], "spl_set_id": ["de8d8007-5718-4fb4-a8c6-4650d2ca9c8f"], "manufacturer_name": ["LiquidCapsule Manufacturing LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "113.4 g in 1 TUBE (71726-004-02)", "package_ndc": "71726-004-02", "marketing_start_date": "20250605"}], "brand_name": "FREEZE IT Menthol", "product_id": "71726-004_6e80d075-fdc1-448f-9e11-7a6980359ef7", "dosage_form": "GEL", "product_ndc": "71726-004", "generic_name": "Menthol", "labeler_name": "LiquidCapsule Manufacturing LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FREEZE IT Menthol", "active_ingredients": [{"name": "MENTHOL", "strength": "3.5 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250605", "listing_expiration_date": "20261231"}