hielo ardiente
Generic: menthol
Labeler: menper distributors, inc.Drug Facts
Product Profile
Brand Name
hielo ardiente
Generic Name
menthol
Labeler
menper distributors, inc.
Dosage Form
GEL
Routes
Active Ingredients
menthol 1 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
53145-002
Product ID
53145-002_3a876b4d-bba4-c8d4-e063-6394a90abaa0
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2012-02-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53145002
Hyphenated Format
53145-002
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
hielo ardiente (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/100g
Packaging
- 454 g in 1 JAR (53145-002-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3a876b4d-bba4-c8d4-e063-6394a90abaa0", "openfda": {"upc": ["0042279419169"], "unii": ["L7T10EIP3A"], "rxcui": ["1039043"], "spl_set_id": ["97ec516c-d2bc-47ce-82fe-bd68445d9570"], "manufacturer_name": ["Menper Distributors, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "454 g in 1 JAR (53145-002-01)", "package_ndc": "53145-002-01", "marketing_start_date": "20120221"}], "brand_name": "Hielo Ardiente", "product_id": "53145-002_3a876b4d-bba4-c8d4-e063-6394a90abaa0", "dosage_form": "GEL", "product_ndc": "53145-002", "generic_name": "Menthol", "labeler_name": "Menper Distributors, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hielo Ardiente", "active_ingredients": [{"name": "MENTHOL", "strength": "1 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120221", "listing_expiration_date": "20261231"}