GOLD ICE Pain Relief

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: GOLD ICE Pain Relief
Generic name: MENTHOL
Manufacturer: Eden's Answers, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: a1356c39-42b9-4bd8-a873-bcd40717058b
SPL ID: 09dc4870-a264-48af-e063-6394a90aa79e
Version: 2
Effective date: 2023-11-11
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:17:49

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		GOLD ICE Pain Relief	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Eden's Answers, Inc.	openfda.manufacturer_name
ndc	package	72226-305-00	openfda.package_ndc
ndc	product	72226-305	openfda.product_ndc
ndc11	package	72226030500	derived:openfda.package_ndc
rxcui		2003750	openfda.rxcui
spl id		09dc4870-a264-48af-e063-6394a90aa79e	id
spl set id		a1356c39-42b9-4bd8-a873-bcd40717058b	set_id
unii		L7T10EIP3A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: For external use only Keep away from fire or flame Flammable: When using this product do not apply to wounds or damaged skin Do not bandage tightly do not use with a heating pad avoid contact with the eyes or mucous membranes use only as directed Stop Use and ask a Doctor if condition worsens symptoms persist for more than 7 days or clears up and occur again within a few days. redness or skin irritation occurs If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.