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

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Clear Anti Itch

Kroger Co
Vi-Jon Inc

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Pramoxind HCl 1%

Zinc acetate 0.1%

Purpose

External analgesic

Skin protectant

Use

  • for the temporary relief oc pain and itching associated with minor skin irritations and rashes due to poison ivy, poison oak or poison sumac
  • dries the oozing and weeping of poison: 
  • ivy
  • oak
  • sumac

Warnings

For external use only

when using this product

do not get into eyes

Stop use and ask a doctor if

  • condition worsens
  • symptoms last 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

  • shake well
  • before applying was affected are of skin

adults and children 2 years of age and older - apply to affected area not more than 3 to 4 times daily

children under 2 years of age - ask a doctor

other information

store at room temperature (59°-77°F)

Inactive ingredients

alcohol , camphor, citric acid, diazolidinyl urea, fragrance, glycerin, hypromellose, methylparaben, oil of lavender, oil of rosemary, polysorbate 40, propylene glycol, propylparaben, purified water, sodium citrate

questions or comments?

1-800-632-6900

Adverse reactions

DISTRIUBTED BY THE KROGER CO

CINCINNATI, OHIO 45202

www.kroger.com

disclaimer

Caladryl Clear is a registered trademark of Johnson + Johnson, Stillman, NJ 08558.  Johnson + Johnson is not affilaed with The Kroger Co. or this product.

Principal Display Panel

COMPARE TO the active ingredients of

CALADRYL CLEAR LOTION  see back panel

Kroger

FROM OUR FAMILY TO YOURS

Clear

anti-itch lotion

  • External Analgesic/Skin Protectant
  • Drying Action Plus Itch Relief

6 FL OZ (177 mL)

Clear Anti Itch

Clear Anti Itch

Pramoxine HCl, Zinc acetate LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:30142-218
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
pramoxine hydrochloride PRAMOXINE 10 mg
ZINC ACETATE zinc 1 mg

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
CAMPHOR (NATURAL)
CITRIC ACID MONOHYDRATE
DIAZOLIDINYL UREA
GLYCERIN
HYPROMELLOSES
METHYLPARABEN
LAVENDER OIL
ROSEMARY OIL
POLYSORBATE 40
propylene glycol
PROPYLPARABEN
water
SODIUM CITRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:30142-218-30 177 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 1994-03-01


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