Mineral Ice Quick Dry Foam

Mineral Ice Quick Dry Foam by

Drug Labeling and Warnings

Mineral Ice Quick Dry Foam by is a Otc medication manufactured, distributed, or labeled by Crown Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MINERAL ICE QUICK DRY FOAM- menthol aerosol, foam 
Crown Laboratories

----------

Mineral Ice Quick Dry Foam

Active Ingredient

Menthol 10%

Purpose

Topical analgesic

Uses

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

● arthritis ● simple backache ● strains

● bruises ● sprains

● provides cooling penetrating relief

Warnings

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

● with other topical pain relievers

● with heating pads or heating devices

When using this product

● 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

condition worsens

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

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions

● 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

● 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

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

Questions?

Call 1-833-279-6522

Additional Information Listed on Other Panels

©2020 Crown Laboratories, Inc.

Distributed by: Crown Laboratories, Inc.

Johnson City, TN 37604 Made in USA

P11842.00 DOT 2Q M5706

Mineral Ice Quick Dry Foam - 4 oz Canister Label

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)

MINERAL ICE QUICK DRY FOAM 
menthol aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0316-0290
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	100 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
2-(DIBUTYLAMINO)ETHYL METHACRYLATE (UNII: XE2SIC67YA)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CETYL ALCOHOL (UNII: 936JST6JCN)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ISOBUTANE (UNII: BXR49TP611)
WATER (UNII: 059QF0KO0R)
N-VINYLCAPROLACTAM (UNII: KFC10CY9UP)
N-VINYLPYRROLIDINONE (UNII: 76H9G81541)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0316-0290-04	113 g in 1 CANISTER; Type 0: Not a Combination Product	04/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/30/2021	07/31/2024

Labeler - Crown Laboratories (079035945)

Registrant - Crown Laboratories (079035945)

Revised: 12/2023

Document Id: 0c930b31-16fe-ef83-e063-6394a90af90d

34390-5

Set id: c3572041-c8cf-162b-e053-2a95a90ad208

Version: 5

Effective Time: 20231215