Anti itch Topical Analgesic description, usages, side effects, indications, overdosage, supplying and lots more!

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Anti itch Topical Analgesic

Chain Drug Marketing Associations Inc




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients                                                                           Purpose

DIPHENHYDRAMINE HYDROCHLORIDE USP, 2%............................. Antihistamine

ZINC ACETATE, 0.1%................................................................. Skin protectant

Purpose

Uses

  • for the temporary relief of itching and pain associated with minor skin irritations and rashes due to insect bites, 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 chicken pox, measles, sunburn, oozing skin, broken blisters, or on extensive areas of the skin more than directed
  • with any other product containing diphenhydramine, even one taken by mouth

When using this product if condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days

Stop use and ask a doctor if condition worsens, or if 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 12 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 12 years of age, consult a doctor

Other information

  • store at 20° to 25°C (68° to 77°F)
  • lot no. & exp. date: see box or see crimp of tube

inactive ingredients

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

DISTRIBUTED BY:

C.D.M.A. INC.

43157 W. NINE MILE

NOVA, MI 48376-0995

Anti itch Topical Analgesic

Anti itch Topical Analgesic

Diphenhydramine Hydrochloride, Zinc Acetate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63868-218
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 2 g
ZINC ACETATE zinc .1 g

Inactive Ingredients

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

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 28 in 1 TUBE
2 NDC:63868-218-01 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2014-02-20


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Be sure to consult your doctor before taking any medication!
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