Label at a glance#

ProductMineral Ice Quick Dry Foam

Active ingredientMENTHOL

Label structure11 sections

Indications and uses

● temporarily relieves minor aches and pains of muscles and joints associated with: ● arthritis ● simple backache ● strains ● bruises ● sprains ● provides cooling penetrating relief

Dosage and administration

● clean affected area before applying product ● hold can at an angle and press nozzle lightly ● dispense onto hand and then apply to target area ● wipe nozzle clean after each use ● replace the overcap after each use ● 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: ask a doctor

Contacts and useful links#

PhoneLabel contact1-833-279-6522

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

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

● arthritis ● simple backache ● strains

● bruises ● sprains

● provides cooling penetrating relief

Warnings

WARNINGS SECTION

For external use only

Contents under pressure. Do not puncture or incinerate. Avoid contact with eyes. If product gets into the eye, flush with water for 15 minutes.

Do not use

OTC - DO NOT USE SECTION

● with other topical pain relievers

● with heating pads or heating devices

When using this product

OTC - WHEN USING SECTION

● do not use in or near the eyes

● do not apply to wounds or damaged skin

● do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

• condition worsens

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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

● clean affected area before applying product ● hold can at an angle and press nozzle lightly ● dispense onto hand and then apply to target area ● wipe nozzle clean after each use ● replace the overcap after each use ● 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: ask a doctor

Other Information

OTHER SAFETY INFORMATION

● store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature] ● do not store at temperatures above 50°C

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aluminum Starch Octenylsuccinate, Caprylyl Glycol, Cetyl Alcohol, Cocamidopropyl Betaine, Ethanol, Isobutane, Phenoxyethanol, Purified Water, Sodium Chloride, Vinyl Caprolactam/VP/Dimethylaminoethyl Methacrylate Copolymer

Questions?

OTC - QUESTIONS SECTION

Call 1-833-279-6522

Additional Information Listed on Other Panels

SPL UNCLASSIFIED SECTION

Distributed by: Crown Laboratories, Inc.

Johnson City, TN 37604 Made in USA

P11842.00 DOT 2Q M5706

RECENT MAJOR CHANGES SECTION

Formatted Uses section

Formatted Directions section

Mineral Ice Quick Dry Foam - 4 oz Canister Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0316-0290-04

NEW

ORIGINAL THERAPEUTIC

Mineral Ice QUICK DRY FOAM

MENTHOL PAIN RELIEVING FOAM

MAXIMUM STRENGTH

Greaseless with DEEPCOLD Pain Reliever

Net wt. 4 oz (113 g)

mineralicefoam

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0316-0290-04	2023-02-13	C162847	48780-1	f386c64a-4245-0266-e053-dadaa90a7c1a	Mineral Ice Quick Dry Foam
0316-0290-04	2023-01-30	C162847	48780-1	f386c64a-4245-0266-e053-dadaa90a7c1a	Mineral Ice Quick Dry Foam

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

Mineral Ice Quick Dry Foam
Menthol
ALCOHOL
PHENOXYETHANOL
2-(DIBUTYLAMINO)ETHYL METHACRYLATE
CAPRYLYL GLYCOL
CETYL ALCOHOL
COCAMIDOPROPYL BETAINE
ISOBUTANE
WATER
N-VINYLCAPROLACTAM
N-VINYLPYRROLIDINONE
ALUMINUM STARCH OCTENYLSUCCINATE
SODIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0316-0290	0316-0290-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
2-(DIBUTYLAMINO)ETHYL METHACRYLATE	XE2SIC67YA	IACT
CAPRYLYL GLYCOL	00YIU5438U	IACT
CETYL ALCOHOL	936JST6JCN	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
ISOBUTANE	BXR49TP611	IACT
WATER	059QF0KO0R	IACT
N-VINYLCAPROLACTAM	KFC10CY9UP	IACT
N-VINYLPYRROLIDINONE	76H9G81541	IACT
MENTHOL	L7T10EIP3A	ACTIB
ALUMINUM STARCH OCTENYLSUCCINATE	I9PJ0O6294	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0c930b31-16fe-ef83-e063-6394a90af90d			c3572041-c8cf-162b-e053-2a95a90ad208	2023-12-15	Warnings	Exact identifier spl id: 0c930b31-16fe-ef83-e063-6394a90af90d spl set id: c3572041-c8cf-162b-e053-2a95a90ad208

Reported adverse events (FAERS/openFDA)#

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