Ice Cold Topical Analgesic Gel description, usages, side effects, indications, overdosage, supplying and lots more!

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Ice Cold Topical Analgesic Gel

Greenbrier International, Inc.




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient                                   Purpose

Menthol 1.25%...........................Topical Analgesic

Purpose

Uses

forthe temporary relief of minor aches and pains of muscles and joints.

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Uses

Other information

  • store at 20oC to 25oC (68o to 77oF)

Warnings

For external use only. Avoid contact with eyes.

Ask a doctor before use if you have cough associated with 

  • smoking
  • excessive phlegm
  • asthma
  • emphysema
  • persistent or chronic cough

When using this product do not

  • heat
  • microwafe
  • add to hot water or any container where healing water may cause splattering and result in burns
  • use in eyes or directly on mucous membranes
  • take by mouth or place in nostrils
  • apply to wounds or damaged skin
  • bandage skin

Consult a doctor and discontinue use if condition worsesn, persists for more than 1 week or tends to recur.

Directions

  • see important warnings under "When using this product"
  • adults & children 2 years of age & older: apply to the affected area not more than 3 to 4 times daily.
  • children under 2 years of age: consult a physician.

Inactive Ingredients

camphor, carbomer, ethyl alcohol, fd&c blue no.1, isopropyl alcohol, methylchloroisothiazolinone, methylisothiazolinone, sodium hydroxide, water.

Ice Cold Topical Analgesic Gel

Ice Cold Topical Analgesic Gel

Menthol GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:33992-3007
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 2.84 mg

Inactive Ingredients

Ingredient Name Strength
water
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)
ALCOHOL
ISOPROPYL ALCOHOL
CAMPHOR (NATURAL)
FD&C BLUE NO. 1
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:33992-3007-1 237 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-05-24


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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