gold ice pain relief
Generic: menthol
Labeler: eden's answers, inc.Drug Facts
Product Profile
Brand Name
gold ice pain relief
Generic Name
menthol
Labeler
eden's answers, inc.
Dosage Form
CREAM
Routes
Active Ingredients
menthol 62.5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72226-305
Product ID
72226-305_09dc4870-a264-48af-e063-6394a90aa79e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2020-08-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72226305
Hyphenated Format
72226-305
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
gold ice pain relief (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 62.5 mg/mL
Packaging
- 1 TUBE in 1 BOX (72226-305-00) / 100 mL in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "09dc4870-a264-48af-e063-6394a90aa79e", "openfda": {"upc": ["0852915003368"], "unii": ["L7T10EIP3A"], "rxcui": ["2003750"], "spl_set_id": ["a1356c39-42b9-4bd8-a873-bcd40717058b"], "manufacturer_name": ["Eden's Answers, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (72226-305-00) / 100 mL in 1 TUBE", "package_ndc": "72226-305-00", "marketing_start_date": "20200801"}], "brand_name": "GOLD ICE Pain Relief", "product_id": "72226-305_09dc4870-a264-48af-e063-6394a90aa79e", "dosage_form": "CREAM", "product_ndc": "72226-305", "generic_name": "MENTHOL", "labeler_name": "Eden's Answers, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GOLD ICE Pain Relief", "active_ingredients": [{"name": "MENTHOL", "strength": "62.5 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}