KIWI CRATE LIQUID HAND - triclosan soap 
Kiwi Crate

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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Active ingredient:
Triclosan 0.3%

Purpose
Antiseptic

Uses: Hand soap to help decrease bacteria on the skin with rinsing by water after use. Recommended for repeated use.

Warnings: For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes.

Do not use in ears or mouth.
When using this product, avoid contact with eyes. In case of contact, flush eyes with water.

Stop use or ask for a doctor if redness or irritation develops and persists for more than 72 hours.

Keep out of reach of children. Children must be supervised in use of this product.

Directions: Pump as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.                                                                                                                                                                          
Other information: Do not store in temperature over 118 F.  

Inactive Ingredients: Water, Sodium Alkyl Ether Sulphate, Cocamidopropyl Betaine, Ammonium Lauryl Sulphate, Disodium Laureth Sulfosuccinate, Cocamide DEA, Sodium Chloride, Fragrance, Methylchloroisothiazolinone, Methylisothiazolinone, Disodium EDTA, Citric Acid, FD&C Red NO.4, FD&C Red NO.33

image of bottle label
KIWI CRATE LIQUID HAND 
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69034-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM C12-15 PARETH-3 SULFATE (UNII: 19Q4RW8UWP)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
COCO DIETHANOLAMIDE (UNII: 92005F972D)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69034-001-1515 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/06/2014
Labeler - Kiwi Crate (030884591)

Revised: 6/2014
Document Id: 8bc84124-769f-4436-8827-e7cdaa83b342
Set id: 4a3beb6f-6e0a-42da-99e5-8e89a6b28715
Version: 1
Effective Time: 20140606
 
Kiwi Crate