Benadryl Original Strength description, usages, side effects, indications, overdosage, supplying and lots more!

Benadryl Original Strength

Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Original Strength BENADRYL ITCH STOPPING CREAM

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
Diphenhydramine hydrochloride 1% Topical analgesic
Zinc acetate 0.1% Skin protectant

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 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 not more than 3 to 4 times daily
  • children under 2 years of age: ask a doctor

Other information

  • store at 20° to 25° C (68° to 77° F)

Inactive ingredients

cetyl alcohol, diazolidinyl urea, methylparaben, polyethylene glycol monostearate 1000, propylene glycol, propylparaben, purified water

Questions?

call 1-800-524-2624 (English/Spanish)

Dist: Johnson & Johnson Consumer Products Company
Division of Johnson & Johnson Consumer Companies Inc.
Skillman, NJ 08558 USA

PRINCIPAL DISPLAY PANEL - 28.3g Tube Carton

ORIGINAL STRENGTH

Benadryl®
Topical Analgesic/Skin Protectant

For ages 2 & up

ITCH
STOPPING
CREAM

NET WT 1 OZ (28.3g)

PRINCIPAL DISPLAY PANEL - 28.3g Tube Carton

Benadryl Original Strength

Diphenhydramine Hydrochloride and Zinc Acetate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:58232-0740
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 10 mg
ZINC ACETATE zinc 1 mg

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 28.3 in 1 TUBE
2 NDC:58232-0740-1 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2012-10-15


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