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itch relief

H E B

HEB Itch Relief Cream Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Diphenhydramine hydrochloride 2%

Zinc acetate 0.1%

Purpose

Topical analgesic

Skin protectant

itch relief 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 areas of the body
  • with any other product containing diphenhydramine, even one taken by mouth

Ask a doctor before use

  • on chicken pox
  • 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
  • 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 than directed
  • adults and children 2 years of age and older: apply to affected area no more than 3 to 4 times daily
  • children under 2 years of age: ask a doctor

itch relief Other information

  • store at 20°-25°C (68°-77°F)

Inactive ingredients

cetyl alcohol, diazolidinyl urea, methylparaben, PEG-2 stearate, PEG-20 stearate, propylene glycol, propylparaben, purified water

Questions or comments? 1-800-719-9260

Principal Display Panel

Compare to active ingredients in Extra Strength Benadryl® Cream

Extra Strength

Itch Relief Cream

2% DIPHENHYDRAMINE HCl and 0.1% ZINC ACETATE

Topical Analgesic & Skin Protectant

itch relief
Itch Relief Cream Carton Image 1 Itch Relief Cream Carton Image 2

itch relief

Diphenhydramine Hydrochloride, Zinc Acetate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37808-622
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
CETYL ALCOHOL
DIAZOLIDINYL UREA
METHYLPARABEN
propylene glycol
PROPYLPARABEN
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 28 in 1 TUBE
2 NDC:37808-622-64 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2010-09-15


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Be sure to consult your doctor before taking any medication!
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