FDA.reportPublic FDA data

Active ingredient

Manufacturer
GLOBAL IMPORT SALES LLC
Effective date
2026-05-25
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-09-22 03:02:15

Label at a glance#

ProductGLOBAL CARE ICE COLD ANALGESIC
Active ingredientMENTHOL
Label structure11 sections

Indications and uses

for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthrists, strains, bruises, sprains

Dosage and administration

adults and children 2 years of age and older, apply to affected area not more than 3 to 4 times daily children under 2 years of age, do not use, consult a doctor

Storage and handling

do not freeze

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1 percent

Purpose

OTC - PURPOSE SECTION

Pain relieving gel

Uses

DOSAGE & ADMINISTRATION SECTION

for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthrists, strains, bruises, sprains

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes
  • do not handage tightly
  • do not apply to wounds or damaged skin
  • do not use with heating pads or other heating devices

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens, or if symptoms persist for more than 7 days or clear up and occur again with a few days. (see other side panel)

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a Posion Control Center immediately

Directions

INDICATIONS & USAGE SECTION

adults and children 2 years of age and older, apply to affected area not more than 3 to 4 times daily

children under 2 years of age, do not use, consult a doctor

Other Information

STORAGE AND HANDLING SECTION

do not freeze

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Ethyl Alcohol, Carbomer, Sodium Hydroxide, Camphor, Methylisothiazolinone, Iodopropynyl Butylcarbamate, FD&C Blue No.1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130870373000965GTIN-13: 0870373000965
EAN-13: 0870373000965
GTIN-12: 870373000965
UPC-A: 870373000965
GTIN storage (14 digits): 00870373000965		00096.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72146-00972146-009-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
METHYLISOTHIAZOLINONE229D0E1QFAIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
WATER059QF0KO0RIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
SODIUM HYDROXIDE55X04QC32IIACT
ALCOHOL3K9958V90MIACT
CARBOMER 934Z135WT9208IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12018-05-01legacy-cache2026-08-02 00:53:54

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6f71833b-d8cf-7f5a-e053-2a91aa0a1b826f71833b-d8ce-7f5a-e053-2a91aa0a1b822018-05-01WarningsExact identifier
spl set id: 6f71833b-d8ce-7f5a-e053-2a91aa0a1b82

Reported adverse events (FAERS/openFDA)#

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