gold ice pain relief

Generic: menthol

Labeler: eden's answers, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name gold ice pain relief
Generic Name menthol
Labeler eden's answers, inc.
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

menthol 62.5 mg/mL

Manufacturer
Eden's Answers, Inc.

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
2003750
UPC
0852915003368
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 gold ice pain relief (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 62.5 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 BOX (72226-305-00) / 100 mL in 1 TUBE
source: ndc

Packages (1)

Ingredients (1)

menthol (62.5 mg/mL)

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"}