Anti-Itch description, usages, side effects, indications, overdosage, supplying and lots more!

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Anti-Itch

Kareway Product, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients (in each gram)

Diphenhydramine HCl 2%

Zinc acetate 0.1%

Purpose

Topical analgesic

Skin protectant

Anti-Itch 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 or 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 areas of the body
  • with any other product containing diphenhydramine, even one taken by mouth

When using this product

  • avoid contact with eyes

Stop use and ask a doctor if

  • condition worsens or does not improve within 7 days
  • 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.

Directions

  • do not use more often than directed
  • 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

Anti-Itch Other information

  • store at 20° - 25°C (68° - 77°F)

Inactive ingredients

Carbomer 940, Cetyl alcohol, Glycerin, Glyceryl monostearate, Light liquid paraffin, Methylparaben, Polysorbate 60, Propylparaben, Purified water, and Stearic acid

Questions or Comments?

1-800-883-0085

Package label

Anti-Itch Cream

Anti-Itch

Anti-Itch

Diphenhydramine HCl, Zinc acetate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67510-0633
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
CARBOMER HOMOPOLYMER TYPE C
CETYL ALCOHOL
GLYCERIN
GLYCERYL MONOSTEARATE
PARAFFIN
METHYLPARABEN
POLYSORBATE 60
STEARIC ACID
PROPYLPARABEN
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 56.6 in 1 TUBE
2 NDC:67510-0633-2 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 2013-12-13


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Be sure to consult your doctor before taking any medication!
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