Mineral Ice Extreme Menthol Pain Relief Spray

Manufacturer
Carlin Consumer Health LLC
Effective date
2026-08-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-08 02:02:11

Label at a glance#

ProductMineral Ice Extreme Menthol Pain Relief
Active ingredientMENTHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Menthol 10.5%

OTC - PURPOSE SECTION

Purpose

Topical analgesic

INDICATIONS & USAGE SECTION

Uses • temporarily relieves minor aches and pains of muscles and joitns associated with:• simple backache • strains • bruises • sprains

WARNINGS SECTION

Warning

For external use only

WARNING Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 50°C (120°F). Keep out of reach of children. WARNING Flammable. Keep away fro mfire or 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 bandage 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 breast feeding, 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 • clean affected area before applying product

• hold can and press nozzle lightly

• apply directly to targeted area

• wipe nozzle clean after each use • replace the overcape after each use

• adults and children 12 years of age and older: spray over affected area not more than 3 to 4 times daily

• children under 12 years of age: consult a physician

Other information

SPL UNCLASSIFIED SECTION

• storea at 20°-25°C (68°-77°F) • do not store at temperatures above 50°C (120°F)

INACTIVE INGREDIENT SECTION

Inactive ingredientsAlcohol Denat., Fragrance, Isopropyl Myristate, Methylsulfonymethane, Water

OTC - QUESTIONS SECTION

Questions? call 1-844-451-1653

SPL UNCLASSIFIED SECTION

@2026 CARLIN CONSUMER HEALTH, LLC

Distributed by: Carlin Consumer Health, LLC

Westport, CT 06880

MineralIceeXtreme.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW

Mineral Ice ®

EXTREME ™

WITH DEEPCOLD ICE MENTHOL

MENTHOL PAIN RELIEF SPRAY

ALPINE FRESH ™ SCENT

4 fl oz (118mL)

labellabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850078192059GTIN-13: 0850078192059
EAN-13: 0850078192059
GTIN-12: 850078192059
UPC-A: 850078192059
GTIN storage (14 digits): 00850078192059
MIN_A7_MineralIceExtreme_SprayCan_PMS306.jpg

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82632-25282632-252-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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 Menthol Pain ReliefMENTHOLCarlin Consumer Health LLC584f5c6e-3385-3221-e063-6294a90aabae2026-08-04WarningsExact identifier
ndc (package): 82632-252-04
ndc (product): 82632-252
ndc11 (package): 82632025204
spl id: 584f5c6e-3386-3221-e063-6294a90aabae
spl set id: 584f5c6e-3385-3221-e063-6294a90aabae

Reported adverse events (FAERS/openFDA)#

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