LEADER ANTI ITCH MAXIMUM STRENGTH description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

LEADER ANTI ITCH MAXIMUM STRENGTH

Cardinal Health

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

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

Uses

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

Other information

  • Store between 20oC and 25oC (68oF and 77oF)

Inactive ingredients

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

DISTRIBUTED BY CARDINAL HEALTH

DULIN, OHIO 43017

CIN 2372134

www.myleader.com

1-800-200-6313

LEADER ANTI ITCH MAXIMUM STRENGTHEnter section text here

LEADER ANTI ITCH MAXIMUM STRENGTH

DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37205-278
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:37205-278-10 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part336 2012-02-10


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.