Mineral Ice Extreme Gel

Manufacturer
Carlin Consumer Health LLC
Effective date
2026-07-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-31 05:10:23

Label at a glance#

ProductMineral Ice Extreme Gel Alpine Fresh Scent
Active ingredientMENTHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Menthol 10%

OTC - PURPOSE SECTION

Purpose

Topical analgesic

INDICATIONS & USAGE SECTION

Uses

• temporarily relieves minor aches and pains of muscles and joints associated with:

• simple backache • strains • bruises • sprains

WARNINGS SECTION

Warnings

For external use only

Flammable: Keep away from excessive heat or open flame

OTC - DO NOT USE SECTION

Do not use

  • with other topical pain relievers
  • with heating pads or heating devices

OTC - WHEN USING SECTION

When using this product

  • avoid contact with eyes
  • do not apply to wounds or damaged skin
  • do not bandge tightly

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

DOSAGE & ADMINISTRATION SECTION

Directions

  • adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 12 years of age: do not use, consult a doctor

Other information

SPL UNCLASSIFIED SECTION

  • store at 20°-25°C (68°-77°F), in a tightly closed container
  • Flammable: Keep away from excessive heat or open flame

INACTIVE INGREDIENT SECTION

Inactive ingredients Alcohol Denat., Aqua (Water), Propylene Glycol, Polyacrylate Crosspolymer-6, Acrylates/C10-30 Alkyl Acrylate Crosspolyer, Aminomethyl Propanol, Ethylhexylglycerin, Lysine, Copper Sulfate, Manganese Chloride, Aluminum Chloride, Gluconolactone, Magnesium Chloride, Potassium Chloride, Phenethyl Alcohol, Sodium Benzoate, Zinc Chloride, Caprylyl Glycol, Calcium Gluconate, Fragrance (Parfum), Phenoxyethanol, Sodium Chloride

OTC - QUESTIONS SECTION

Questions or comments? call 1-844-451-1653

SPL UNCLASSIFIED SECTION

@2026 CARLIN CONSUMER HEALTH, LLC

Distributed by:

Carlin Consumer Health, LLC

Westport, CT 06880

MADE IN CANADA

MineralIceXtreme.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mineral

Ice ®

EXTREME ™

WITH DEEPCOLD ®

ICE MENTHOL

MENTHOL

PAIN

RELIEF

GEL

ALPINE FRESH ™ SCENT

4 FL OZ (118 mL)

labellabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850078192035GTIN-13: 0850078192035
EAN-13: 0850078192035
GTIN-12: 850078192035
UPC-A: 850078192035
GTIN storage (14 digits): 00850078192035
253 label.jpg

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82632-25382632-253-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

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
Mineral Ice Extreme Gel Alpine Fresh ScentMENTHOLCarlin Consumer Health LLC56d3ca3d-21e1-a40a-e063-6294a90a9ff42026-07-17WarningsExact identifier
ndc (package): 82632-253-01
ndc (product): 82632-253
ndc11 (package): 82632025301
spl id: 56d3ca3d-21e2-a40a-e063-6294a90a9ff4
spl set id: 56d3ca3d-21e1-a40a-e063-6294a90a9ff4

Reported adverse events (FAERS/openFDA)#

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