MINERAL ICE PAIN RELIEVING- menthol gel 
Crown Laboratories

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Mineral Ice

Active ingredient

Menthol 2%

Purpose

Topical analgesic

Uses

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

● arthritis ● simple backache ● strains

● provides cooling penetrating relief

Warnings

For external use only

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

Other information

Inactive ingredients

ammonium hydroxide, carbomer, cupric sulfate, FD&C blue no. 1, isopropyl alcohol, magnesium sulfate, purified water, sodium hydroxide, thymol

Questions or comments?

call 1-833-279-6522

Additional Information Listed on Other Panels

1-833-279-6522 ©Crown Laboratories, Inc.

Distributed by: Crown Laboratories, Inc.

Johnson City, TN 37604 ©2018 Made in Canada.

Mineral Ice and the Mineral Ice mountain range are registered trademarks of Crown Laboratories, Inc.

Principal Display

NDC 0316-0226-08

ORIGINAL THERAPEUTIC

Mineral Ice®

Menthol Pain Relieving Gel

Greaseless with DEEPCOLD® Pain Reliever

Net wt. 8 oz (226.8 g)

P11529.00

p1152900

MINERAL ICE  PAIN RELIEVING
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-0226
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
AMMONIA (UNII: 5138Q19F1X)  
CARBOMER HOMOPOLYMER TYPE B (UNII: HHT01ZNK31)  
CUPRIC SULFATE (UNII: LRX7AJ16DT)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
THYMOL (UNII: 3J50XA376E)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-0226-3599.2 g in 1 JAR; Type 0: Not a Combination Product12/01/2018
2NDC:0316-0226-08226.8 g in 1 JAR; Type 0: Not a Combination Product12/01/2018
3NDC:0316-0226-16453.6 g in 1 JAR; Type 0: Not a Combination Product12/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01711/01/2011
Labeler - Crown Laboratories (079035945)

Revised: 11/2023
Document Id: 0a5be3d9-8fe1-03c2-e063-6294a90a7d56
Set id: 7b30076a-0af6-2f74-e053-2a91aa0ae08d
Version: 8
Effective Time: 20231117
 
Crown Laboratories