ANTIBACTERIAL FOAMING description, usages, side effects, indications, overdosage, supplying and lots more!

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ANTIBACTERIAL FOAMING

Topco Associates LLC
APOLLO HEALTH AND BEAUTY CARE

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

TRICLOSAN 0.6 PERCENT

PURPOSE

ANTIBACTERIAL

USES

HELPS REDUCE BACTERIA ON THE SKIN.

WARNINGS

FOR EXTERNAL USE ONLY.

KEEP OUT OF REACH OF CHILDREN

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES.  IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.

STOP USING THIS PRODUCT AND ASK DOCTOR IF

IRRITATION AND REDNESS DEVELOPS AND LASTS.

DIRECTIONS

PUMP ONTO DRY HANDS, WORK INTO A LATHER AND RINSE THOROUGHLY.

STORE AT ROOM TEMPERATURE.

INACTIVE INGREDIENTS


FRONT AND BACK LABELS

ANTIBACTERIAL FOAMING

ANTIBACTERIAL FOAMING

TRICLOSAN LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:36800-076
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TRICLOSAN TRICLOSAN 0.6 mL

Inactive Ingredients

Ingredient Name Strength
SODIUM XYLENESULFONATE
DIPROPYLENE GLYCOL
SODIUM LAURETH SULFATE
COCAMIDOPROPYL BETAINE
sodium phosphate, dibasic, dihydrate
CITRIC ACID MONOHYDRATE
D&C RED NO. 33
FD&C YELLOW NO. 5
water
POLYSORBATE 20
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:36800-076-08 222 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2011-11-02


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