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

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CAREONE

American Sales Company
APOLLO HEALTH AND BEAUTY CARE

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

TRICLOSAN 0.46%

PURPOSE

ANTIBACTERIAL

USES

FOR WASHIG TO DECREASE BACTERIA ON THE SKIN

WARNINGS

FOR EXTERNAL USE ONLY

WHEN USING THIS PRODUCT

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

STOP USING THIS PRODUCT AND ASK A DOCTOR IF

IRRITATION OR REDNESS DEVELOPS AND LASTS MORE THAN 7 DAYS

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

APPLY TO DRY HANDS, WORK INTO A RICH FOAMY LATHER AND RINSE THOROUGHLY

OTHER INFORMATION

STORE AT ROOM TEMPERATURE

INACTIVE INGREDIENTS

WATER, SODIUM LAURETH SULFATE, DISODIUM LAURETH SULFOSUCCINATE, COCAMIDOPROPYLAMINE OXIDE, PPG-1-PEG-9 LAURYL GLYCOL ETHER, FRAGRANCE (PARFUM), PEG-7 GLYCERYL COCOATE, BENZOPHENONE-4, GLYCERIN, TETRASODIUM EDTA, SODIUM CHLORIDE, BENZYL ALCOHOL, GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE, CAMELLIA SINENSIS LEAF EXTRACT, ALOE BARBADENSIS LEAF JUICE, VANILLA PLANIFOLIA FRUIT EXTRACT, PROPYLENE GLYCOL, HYDROXYPROPYL METHYLCELLULOSE, CITRIC ACID, SODIUM HYDROXIDE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, YELLOW 5 (CI 19140), RED 33 (CI 17200), BLUE 1 (CI 42090)

LABEL COPY

CAREONE

CAREONE

TRICLOSAN LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41520-107
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TRICLOSAN TRICLOSAN 4.6 mg

Inactive Ingredients

Ingredient Name Strength
water
SODIUM LAURETH SULFATE
disodium laureth sulfosuccinate
COCAMIDOPROPYLAMINE OXIDE
PEG-7 GLYCERYL COCOATE
SULISOBENZONE
GLYCERIN
EDETATE SODIUM
SODIUM CHLORIDE
BENZYL ALCOHOL
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)
GREEN TEA LEAF
Aloe Vera Leaf
VANILLA
propylene glycol
HYPROMELLOSES
CITRIC ACID ACETATE
SODIUM HYDROXIDE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
FD&C YELLOW NO. 5
D&C RED NO. 33
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:41520-107-08 237 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2014-02-06


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