OTC Medication Information: CACTUS FLOWER AND MANGO ANTIBACTERIAL DEEP CLEANSING HAND SP

CACTUS FLOWER AND MANGO ANTIBACTERIAL DEEP CLEANSING HAND SP — triclosan liquid
HEB

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

ACTIVE INGREDIENT

TRICLOSAN 0.3 PERCENT

PURPOSE

ANTIBACTERIAL

USES

TO HELP REDUCE BACTERIA ON THE SKIN.

WARNINGS

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

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

STOP USING THIS PRODUCT AND ASK DOCTOR IF

IRRITATION OR REDNESS DEVELOPS AND LASTS.

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

APPLY TO WET HANDS, LATHER AND RINSE THOROUGHLY.

QUESTIONS OR COMMENTS

1-866-695-3030

INACTIVE INGREDIENTS

WATER, SODIUM LAURETH SULFATE, ACRYLATES COPOLYMER, COCAMIDOPROPYL BETAINE, COCAMIDE DEA, SODIUM CHLORIDE, FRAGRANCE, ALOE BARBADENSIS LEAF JUICE, PEG-7 GLYCERYL COCOATE, HELIANTHUS ANNUUS (SUNFLOWER) EXTRACT, CEREUS GRANDIFLORUS (CACTUS) FLOWER EXTRACT, MANGIFERA INDICA (MANGO) FRUIT EXTRACT, POLYETHYLENE, TETRASODIUM EDTA, SODIUM STYRENE/PEG-10 MALEATE/NONOXYNOL-10 MALEATE/ACRYLATES COPOLYMER, AMMONIUM NONOXYNOL-4 SULFATE, CITRIC ACID, SODIUM HYDROXIDE, MANNITOL, CELLULOSE, HYDROXYPROPYL METHYLCELLULOSE, MICA, TITANIUM OXIDE (CI 77891), IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), YELLOW 5 (CI 19140), RED 4 (CI 14700), RED 33 (CI 17200), METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE.

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CACTUS FLOWER AND MANGO ANTIBACTERIAL DEEP CLEANSING HAND SP
triclosan liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-291
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICLOSAN (TRICLOSAN) TRICLOSAN 0.3 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
SODIUM LAURETH SULFATE
CARBOMER COPOLYMER TYPE A
COCAMIDOPROPYL BETAINE
COCO DIETHANOLAMIDE
SODIUM CHLORIDE
ALOE VERA LEAF
GLYCERYL COCOATE
HELIANTHUS ANNUUS FLOWER
SELENICEREUS GRANDIFLORUS FLOWER
MANGO
LOW DENSITY POLYETHYLENE
EDETATE SODIUM
NONOXYNOL-10
AMMONIUM NONOXYNOL-4 SULFATE
ANHYDROUS CITRIC ACID
SODIUM HYDROXIDE
MANNITOL
POWDERED CELLULOSE
HYPROMELLOSES
MICA
TITANIUM DIOXIDE
FERRIC OXIDE RED
FD&C YELLOW NO. 5
FD&C RED NO. 4
D&C RED NO. 33
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
FERRIC OXIDE YELLOW
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37808-291-08 236 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 12/30/2010
Labeler — HEB (007924756)
Registrant — APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
Name Address ID/FEI Operations
APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture

Revised: 12/2010 HEB

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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