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

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Clear Anti Itch

/Vi-Jon
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 of 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

Disclaimer

This product is not manufactured or distributed by Pfizer Consumer HealthCare, distributor of Caladryl Clear

DSP-TN-15000

DSP-MO-34

SDS-TN-15012

Adverse reactions

Vi-Jon

One Swan Drive

Smyrna, TN 37167

Principal Display Panel

SWAN

Clear

Anti-itch

Lotion

EXTERNAL ANALGESIC

SKIN PROTECTANT

For Relief from Pain and Itchind due to:

Poison Ivy, Poison Sumac, Insect Bites, Poison Oak, + Minor Skin Irritatins

Compare to the active ingredients of Caladryl Clear

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:0869-0218
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:0869-0218-30 177 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 1994-05-07


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Be sure to consult your doctor before taking any medication!
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