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

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Caladryl Clear

Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

Caladryl Clear


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
Pramoxine HCl 1% Topical analgesic
Zinc acetate 0.1% Skin protectant

Caladryl Clear Uses

  • temporarily relieves pain and itching associated with:
    • rashes due to poison ivy, poison oak or poison sumac
    • insect bites
    • minor skin irritation
    • minor cuts
  • dries the oozing and weeping of poison ivy, poison oak and poison sumac

Warnings

For external use only.

When using this product do not get into eyes

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

  • shake well before use
  • 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

Caladryl Clear Other information

  • store at 20° to 25°C (68° to 77°F)

Inactive ingredients

SD alcohol 38-B, camphor, citric acid, diazolidinyl urea, fragrance, glycerin, hypromellose, methylparaben, polysorbate 40, propylene glycol, propylparaben, purified water, sodium citrate

Questions?

call 1-800-223-0182

Dist: Johnson & Johnson Consumer Products Company Division of Johnson & Johnson Consumer Companies Inc. Skillman, NJ 08558 USA

PRINCIPAL DISPLAY PANEL - 177 mL Bottle Label

Caladryl®
Clear®
Topical Analgesic ∙ Skin Protectant
Lotion

Drying Action PLUS Itch Relief

6 FL OZ (177 mL)

Caladryl Clear

Caladryl Clear

PRAMOXINE HYDROCHLORIDE and ZINC ACETATE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:58232-0731
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
CAMPHOR (SYNTHETIC)
CITRIC ACID MONOHYDRATE
DIAZOLIDINYL UREA
GLYCERIN
HYPROMELLOSES
METHYLPARABEN
POLYSORBATE 40
propylene glycol
PROPYLPARABEN
water
SODIUM CITRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:58232-0731-6 177 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 2012-02-17


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Be sure to consult your doctor before taking any medication!
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