CAREONE ALLERGY description, usages, side effects, indications, overdosage, supplying and lots more!

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CAREONE ALLERGY

American Sales Company

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients                                                                            Purpose

Diphenhydramine Hydrochloride 2% .........................................Topical analgesic

Zinc acetate, 0.1% .........................................................................Skin Protectant

Purpose

Uses

Temporarily relieves pain and itching associated with: insect bites, minor burns, sunburn, minor skin irritations, minor cuts, scrapes, rashes due to poison ivy, poison oak, and poison sumac. Dries the oozing and weeping of poison ivy, poison oak, and poison sumac.

Warnings

For external use only

Do not use on large area of the body or with any other product containing diphenhydramine, even one taken by mouth.

Ask a doctor before use

on chicken pox or on measles.

When using this product

avoid contact with the eyes.

Stop use and ask a doctor if condition worsens or does not improve within 7 days, or symptoms persist for more than 7 days, or clear up and occur again within a few days.

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Directions

  • do not use more than directed
  • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily, or as directed by a doctor
  • children under 2 years of age: consult a doctor
  • discontinue use and consult a physician if rash or irritation develops

Other information

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

Inactive ingredients

cetanol, methylparaben, polyoxyl 40 stearate, propylene glycol, propylparaben, purified water, stearyl alcohol

DISTRIBUTED BY

AMERICAN SALES COMPANY

4201 WALDEN AVENUE

LANCASTER, NY 14086

Made in Korea

CAREONE ALLERGYEnter section text here

CAREONE ALLERGY

DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41520-314
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 2 g
ZINC ACETATE zinc 0.1 g

Inactive Ingredients

Ingredient Name Strength
METHYLPARABEN
POLYOXYL 40 STEARATE
propylene glycol
PROPYLPARABEN
water
stearyl alcohol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 28 in 1 TUBE
2 NDC:41520-314-28 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2012-03-01


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