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

Menu
Search

Itch Relief

Safetec of America, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredients

Diphenhydramine hydrochloride 2%

Purpose

External Analgesic

Uses:

For the temporary relief of pain and itching associated with minor skin irritations and rashes due to insect bites, poison oak and poison sumac.

Warnings

For external use only

Do not use

  • on large areas of the body
  • with any other products using diphenhydramine hydrochloride, even one taken by mouth

Ask a doctor before use

  • on chicken pox
  • on measles

When using this product

  • avoid contact with the eyes

Stop use and ask doctor if

  • condition worsens
  • symptoms persist 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 center right away.

Directions:

  • 12 and over: apply to affected area not more than 3 to 4 times daily
  • under 12: consult a doctor

Inactive Ingredients:

Germaben II, edetate disodium, glycerin, tomadol 25-9, purified water, triethanolamine

PRINCIPAL DISPLAY PANEL

NDC 61010-8300-1

Safetec

Diphenhydramine

Itch Relief Spray

Relief from pain and

itching due to insect

bites and rashes from

poison ivy, poison oak

and poison sumac.

Manufactured by

SAFETEC OF AMERICA, Inc.

Buffalo, NY 14215 800-456-7077

www.safetec.com

2 fl. oz. (59.1ml) Reorder no. 57001

Itch Relief

diphenhydramine hydrochloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:61010-8300
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 20.3 g

Inactive Ingredients

Ingredient Name Strength
DIAZOLIDINYL UREA
EDETATE DISODIUM
GLYCERIN
C12-15 PARETH-9
water
TROLAMINE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61010-8300-1 0.0591 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-05-02


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.