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

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Anti-Itch

Navarro Discount Pharmacies,LLC

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients (in each gram)

Diphenhydramine HCl 2%

Purposes

Topical analgesic

Skin protectant

Anti-Itch Uses

  • temporarily relieves itching and pain associated with insect bites, minor skin irritations and rashes due to poison ivy, poison oak or 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 or measles
  • with any other product containing diphenhydramine, even one taken by mouth
  • on large areas of the body, including large areas of poison ivy, sunburn, or broken, blistered or oozing skin

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

  • adults and children 12 years of age and over:  apply to affected area not more than 3 to 4 times daily
  • children under 12 years of age:  ask a doctor
  • do not use more often than directed

Anti-Itch Other information

  • store at 15°-25°C (59°-77°F)

Inactive ingredients

camphor, citric acid, ethanol, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate

Package label

Anti-Itch GelAnti-Itch

Anti-Itch

Diphenhydramine HCl GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59970-076
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
CAMPHOR (SYNTHETIC)
CITRIC ACID MONOHYDRATE
ALCOHOL
GLYCERIN
METHYLPARABEN
propylene glycol
PROPYLPARABEN
water
SODIUM CITRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59970-076-01 113 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part336 2013-01-18


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Be sure to consult your doctor before taking any medication!
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