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#
Contacts and useful links#
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
• 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)
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0850078192059 | GTIN-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.
- Mineral Ice Extreme Menthol Pain Relief
- Menthol
- ALCOHOL
- ISOPROPYL MYRISTATE
- METHOSULFONYLMETHANE
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82632-252 | 82632-252-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MENTHOL | L7T10EIP3A | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
| ISOPROPYL MYRISTATE | 0RE8K4LNJS | IACT |
| METHOSULFONYLMETHANE | 9H4PO4Z4FT | IACT |
| WATER | 059QF0KO0R | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Mineral Ice Extreme Menthol Pain Relief | MENTHOL | Carlin Consumer Health LLC | 584f5c6e-3385-3221-e063-6294a90aabae | 2026-08-04 | Warnings | 82632-252-04 82632-252 82632025204 584f5c6e-3386-3221-e063-6294a90aabae 584f5c6e-3385-3221-e063-6294a90aabae |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
