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

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Bite and Itch

Weeks & Leo Co., Inc.
DSC Laboratories, Div. of DSC Products Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients






Purpose

Topical Analgesic

Topical Analgesic

Bite and Itch Uses

temporarily relieves pain and itching due to:

  • scrapes
  • minor burns
  • poison ivy, poison oak, or poison sumac
  • sunburn
  • insect bites
  • minor cuts
  • minor skin irritations

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 if you have

  • chicken pox
  • measles

When using this product

do not get into eyes

Stop use and ask a doctor if

  • condition gets worse
  • symptoms last for more than 7 days 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 often than directed
  • adults and children 12 years and over: apply to affected areanot more than 3 to 4 times daily
  • children under 12 years: ask a doctor

Bite and Itch Other information

  • store at controlled room temperature

Inactive ingredients

cetyl alcohol, glyceryl monostearate, isopropyl myristate, menthol, mineral oil, polysorbate 60, propylene glycol, purified water, sodium benzoate, stearyl alcohol

Bite and Itch Lotion 4 oz Labeling


Bite and Itch

This product is also labeled as Solarhist Lotion. All other labeling and packaging is the same.

Labeled and Dist. by:

Weeks and Leo Co. Inc.

Des Moines, IA 50322

Bite and Itch Lotion 4oz

Bite and Itch

Diphenhydramine HCl and Pramoxine HCl LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11383-193
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 20 mg
pramoxine hydrochloride PRAMOXINE 10 mg

Inactive Ingredients

Ingredient Name Strength
CETYL ALCOHOL
GLYCERYL MONOSTEARATE
ISOPROPYL MYRISTATE
MENTHOL
Mineral Oil
POLYSORBATE 60
propylene glycol
SODIUM BENZOATE
stearyl alcohol
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11383-193-04 113 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2000-01-06


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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