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

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XtraCare Ice Cold Topical Analgesic Gel

China Ningbo Shangge Cosmetic Technology Corp




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients:                                  Purpose

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

Purpose

Uses

for the 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

XtraCare® Ice Cold Topical Analgesic Gel

Net Wt 8 oz (227 g)

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
  • microwave
  • add to hot water or any container where heating 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 worsens, 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.

Other information:  store at 20o to 25oC (68o to 77oF)

Questions/Comments?  1-855-345-5575

DISTRIBUTED BY:

REJOICE INTERNATIONAL INC

NORTHVILLE, MI 48168 USA

MADE IN CHINA

XtraCare Ice Cold Topical Analgesic Gel

XtraCare Ice Cold Topical Analgesic Gel

Menthol GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:58503-052
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 3 g

Inactive Ingredients

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

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:58503-052-01 227 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2014-01-30


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