Calamine Phenolated Topical Suspension description, usages, side effects, indications, overdosage, supplying and lots more!

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Calamine Phenolated Topical Suspension

Humco Holding Group, Inc
Humco Holding Group, Inc.

Calamine PhenolatedTopical Suspension USP


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredient

Calamine 8%

Purpose

Skin Protectant

Active Ingredient

Zinc Oxide 8%

Purpose

Skin Protectant

Active Ingredient

Liquefied Phenol

Purpose

Topical Analgesic

Calamine Phenolated Topical Suspension Uses

Dries the oozing and weeping and temporarily pain and itching of poison ivy, poison oak, and poison sumac, or other minor skin irritations

Warnings

  • For external use only. Use only as directed.
  • Avoid contact with eyes and mucous membranes.
  • Do not apply to large areas of the body or in large quantities, particularly over raw or blistered areas.
  • If applied to fingers or toes do not bandage.

before using on children under 2 years of age.

When using this product. Discontinue use if condition worsen or does not improve within 7 days and consult a doctor.

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a poison Control Center immediately.

directions (Shake well before using)

Adult and children 2 years of age and older: Cleanse the skin with soap and water and let dry before each use. Apply product to the affected area using cotton or soft cloth, as often as needed for comfort.

Children under 2 years of age: Consult a doctor before use.

Other Information.

Store at room temperature 15-30C (59-86F)

Inactive Ingredients.

Bentonite Magma, Calcium Hydroxide, Glycerin, Purified Water.

Questions or Comments?

1-800-662-3435  www.goodneighborpharmacy.com

Principal Display Panel

Label

Calamine Phenolated Topical Suspension

Calamine Phenolated Topical Suspension

Calamine and Zinc Oxide and Phenol LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0395-0407
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Zinc Oxide Zinc oxide 160 mg
PHENOL 10 mg

Inactive Ingredients

Ingredient Name Strength
BENTONITE
Calcium Hydroxide
GLYCERIN
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0395-0407-96 177 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part347 1998-03-25


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