Mineral Ice Extreme Dry Stick

Manufacturer: Carlin Consumer Health LLC
Effective date: 2026-06-02
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: daily-update
Hydrated at: 2026-08-11 01:01:09

Label at a glance#

ProductMineral Ice Extreme Dry Stick

Active ingredientMENTHOL

Label structure11 sections

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact1-844-451-1653

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Menthol 16%

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 • provides cooling, penetrating relief

WARNINGS SECTION

Warnings

For external use only

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 preganant or breast feeding, as 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: turn dial and apply a thin film by rubbing over affected area not more than 3 to 4 times a day.

Other information

SPL UNCLASSIFIED SECTION

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

INACTIVE INGREDIENT SECTION

Inactive ingredients C15-19 Alkane, Fragrance, Hydrogenated Castor Oil, Lauryl Laurate, Menthoxypropanediol, Oleic Acid, Paraffin, Petrolatum, Tocopheryl Acetate, Fragrance @ 2.0%

OTC - QUESTIONS SECTION

Questions?call 1-844-451-1653

SPL UNCLASSIFIED SECTION

Distributed by: Carlin Consumer Health, LLC

Westport, CT 06880. MADE IN CANADA

MinerallceXtreme.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mineral Ice ^®

EXTREME™

MAXIMUM

STRENGTH

ALPINE FRESH™ SCENT

DRY STICK NET WT. 3oz (85 g)

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

Products#

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

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

Mineral Ice Extreme Dry Stick
menthol
C15-19 ALKANE
ALPHA-TOCOPHEROL ACETATE
PARAFFIN
LAURYL LAURATE
PETROLATUM
OLEIC ACID
HYDROGENATED CASTOR OIL
MENTHOXYPROPANEDIOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
82632-250	82632-250-05, 82632-250-04

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
Name	UNII	Kind
C15-19 ALKANE	CI87N1IM01	IACT
ALPHA-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
MENTHOL	L7T10EIP3A	ACTIB
PARAFFIN	I9O0E3H2ZE	IACT
LAURYL LAURATE	GPW77G0937	IACT
PETROLATUM	4T6H12BN9U	IACT
OLEIC ACID	2UMI9U37CP	IACT
HYDROGENATED CASTOR OIL	ZF94AP8MEY	IACT
MENTHOXYPROPANEDIOL	KD6TZ2QICH	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
1	2026-04-01	full-release	2026-06-01 01:53:54

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mineral Ice Extreme Dry Stick	MENTHOL	Carlin Consumer Health LLC	4f81be91-92e5-1205-e063-6394a90a6e82	2026-06-02	Warnings	Exact identifier ndc (package): 82632-250-04 ndc (package): 82632-250-05 ndc (product): 82632-250 ndc11 (package): 82632025005 ndc11 (package): 82632025004 spl id: 53464550-4096-d2cb-e063-6394a90aa89e spl set id: 4f81be91-92e5-1205-e063-6394a90a6e82

Reported adverse events (FAERS/openFDA)#

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