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

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Itch Relief

Water-Jel Technologies
Water-Jel Technologies

Itch Relief


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Diphenhydramine hydrochloride 2%

Purpose

External analgesic

Itch Relief Uses

for temporary relief of pain and itching associated with minor burns, minor cuts, scrapes, insect bites or minor skin irritations

Warnings

For external use only

Do not use

  • on poison ivy or sunburn
  • on broken, blistered or oozing skin
  • 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 or measles

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

Keep out of the 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 the affected area not more than 3 - 4 times daily
  • children under 2 years: consult a doctor

Itch Relief Other information

  • store at room temperature

Inactive ingredients

diazoldinyl urea, edetate disodium, glycerin, hypromellose, methylparaben, octoxynol 9, propylene glycol, propylparaben, purified water, trolamine

Questions or comments?

1-800-275-3433   info@waterjel.com   www.waterjel.com

Principal Display Panel

Itch Relief

Itch Relief

Diphenhydramine Hydrochloride SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59898-810
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 2 g

Inactive Ingredients

Ingredient Name Strength
DIAZOLIDINYL UREA
EDETATE DISODIUM
hypromellose
METHYLPARABEN
octoxynol 9
propylene glycol
PROPYLPARABEN
water
TROLAMINE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59898-810-10 59 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2010-09-25


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Be sure to consult your doctor before taking any medication!
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