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

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ANTIBACTERIAL

SAM'S WEST INC.
APOLLO HEALTH AND BEAUTY CARE

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

TRICLOSAN 0.115 PERCENT

PURPOSE

ANTIBACTERIAL

USES

FOR HANDWASHING TO DECREASE BACTERIA ON THE SKIN.

WARNINGS

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

DO NOT GET INTO EYES.  IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER.

KEEP OUT OF REACH OF CHILDREN.

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

STOP USING THIS PRODUCT AND ASK A DOCTOR IF

IRRITATION OR REDNESS DEVELOPS AND LASTS.

DIRECTIONS:

  • WET HANDS
  • APPLY PALMFUL TO  HANDS
  • SCRUB THOROUGHLY
  • RINSE

INACTIVE INGREDIENTS

WATER, SODIUM LAURETH SULFATE, LAURAMIDE DEA, COCAMIDOPROPYL BETAINE, DECYL GLUCOSIDE, POLYQUATERNIUM-7, SACCHAROMYCES,  HYDROLYZED VEGETABLE PROTEIN, CAMELLIA SINENSIS (GREEN TEA) LEAF EXTRACT, SODIUM BICARBONATE, ALOE BARBADENSIS LEAF JUICE, TOCOPHERYL ACETATE, RETINYL PALMITATE, ASCORBYL PALMITATE, NIACINAMIDE, TETRASODIUM EDTA, SODIUM CHLORIDE, FRAGRANCE, DMDM HYDANTOIN, CITRIC ACID, RED 33 (CI 17200), BLUE 1 (CI 42090).

ANTIBACTERIAL

ANTIBACTERIAL

TRICLOSAN LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68196-143
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TRICLOSAN TRICLOSAN 0.115 L

Inactive Ingredients

Ingredient Name Strength
water
SODIUM LAURETH SULFATE
LAURIC DIETHANOLAMIDE
COCAMIDOPROPYL BETAINE
LAURYL GLUCOSIDE
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD)
SACCHAROMYCES LYSATE
SOY PROTEIN
SODIUM BICARBONATE
Aloe Vera Leaf
.ALPHA.-TOCOPHEROL ACETATE, D-
VITAMIN A PALMITATE
ASCORBYL PALMITATE
NIACINAMIDE
EDETATE SODIUM
SODIUM CHLORIDE
DMDM HYDANTOIN
ANHYDROUS CITRIC ACID
D&C RED NO. 33
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68196-143-80 2.36 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2011-06-06


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