ORCHID BY H E B VANILLA BROWN SUGAR- triclosan liquid 
H E B

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.

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DRUG FACTS

ACTIVE INGREDIENT

TRICLOSAN 0.46%

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 DRY HANDS, LATHER AND RINSE THOROUGHLY

QUESTIONS/COMMENTS?

1-866-695-3030

INACTIVE INGREDIENTS

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

LABEL COPY

IMAGE OF THE LABEL

ORCHID BY H E B  VANILLA BROWN SUGAR
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-107
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN4.6 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L)  
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
GLYCERIN (UNII: PDC6A3C0OX)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SULIBENZONE (UNII: 853Z42ZYAS)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
VANILLA (UNII: Q74T35078H)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-107-08236 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/03/2014
Labeler - H E B (007924756)
Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
Establishment
NameAddressID/FEIBusiness Operations
APOLLO HEALTH AND BEAUTY CARE201901209manufacture(37808-107)

Revised: 3/2014
Document Id: 5c8ffeb0-67a2-46b8-9217-483fb7a67183
Set id: 32716b5c-0855-4ff0-a29d-747aec8fe53d
Version: 1
Effective Time: 20140304
 
H E B