Mineral Ice description, usages, side effects, indications, overdosage, supplying and lots more!

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Mineral Ice

Novartis Consumer Health, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient  

Menthol 2%

Purpose

Topical analgesic

Mineral Ice Uses

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

● arthritis ● simple backache ● strains

  •  ● bruises ● sport injuries ● sprains

● 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
  • redness or irritation develops

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
  • 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

Mineral Ice Other information

  • store in a cool place
  • keep lid tightly closed
  • do not use, pour, spill or store near heat or open flame

Inactive ingredients

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

Questions or comments?

call 1-800-468-7746

Additional Information Listed on Other Panels

Distributed by: Novartis Consumer Health, Inc.

Parsippany, NJ 07054-0622 ©20XX Made in Canada.

 

ORIGINAL THERAPEUTIC

Mineral Ice®

Pain Relieving Gel

Greaseless with DEEPCOLD® Pain Reliever

Principal Display

Mineral Ice
Mineral Ice Label

Mineral Ice

Menthol GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0067-2067
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL .02 g

Inactive Ingredients

Ingredient Name Strength
AMMONIA
CARBOMER HOMOPOLYMER TYPE B
CUPRIC SULFATE
FD&C BLUE NO. 1
ISOPROPYL ALCOHOL
Magnesium Sulfate Heptahydrate
SODIUM HYDROXIDE
THYMOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0067-2067-35 99.2 in 1 JAR
2 NDC:0067-2067-08 226.8 in 1 JAR
3 NDC:0067-2067-16 453.6 in 1 JAR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2011-11-01


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Be sure to consult your doctor before taking any medication!
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