sunmed pain freeze

Generic: menthol

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

Drug Facts

Product Profile

Brand Name sunmed pain freeze
Generic Name menthol
Labeler sunflora inc.
Dosage Form SPRAY
Routes
TOPICAL
Active Ingredients

menthol 6 g/100mL

Manufacturer
Sunflora Inc.

Identifiers & Regulatory

Product NDC 73240-904
Product ID 73240-904_3cbd785f-2ab1-56e2-e063-6294a90a65fc
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017.10
Listing Expiration 2026-12-31
Marketing Start 2025-08-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73240904
Hyphenated Format 73240-904

Supplemental Identifiers

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 sunmed pain freeze (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017.10 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 6 g/100mL
source: ndc
Packaging
  • 89 mL in 1 BOTTLE, PLASTIC (73240-904-01)
source: ndc

Packages (1)

73240-904-01 89 mL in 1 BOTTLE, PLASTIC (73240-904-01)

Ingredients (1)

menthol (6 g/100mL)

Linked Drug Pages (1)

SUNMED pain freeze ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3cbd785f-2ab1-56e2-e063-6294a90a65fc", "openfda": {"unii": ["L7T10EIP3A"], "spl_set_id": ["ff49699c-ced9-13d2-e053-6394a90af079"], "manufacturer_name": ["Sunflora Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "89 mL in 1 BOTTLE, PLASTIC (73240-904-01)", "package_ndc": "73240-904-01", "marketing_start_date": "20250819"}], "brand_name": "SUNMED pain freeze", "product_id": "73240-904_3cbd785f-2ab1-56e2-e063-6294a90a65fc", "dosage_form": "SPRAY", "product_ndc": "73240-904", "generic_name": "MENTHOL", "labeler_name": "Sunflora Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUNMED pain freeze", "active_ingredients": [{"name": "MENTHOL", "strength": "6 g/100mL"}], "application_number": "M017.10", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250819", "listing_expiration_date": "20261231"}