CHLOROXYLENOL 0.3%- chloroxylenol 0.3% liquid 
CVS Pharmacy

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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Crisp Green Apple Antibacterial Hand Soap
956.002/956AD rev 1-AE rev 1

Disclaimer

Do not add bleach

Not for use in dishwasher

Contains Surfactants    Phosphate Free

*This product is not manufactured or distributed by Procter & Gamble, owner of the registered trademark Dawn.

Active ingredient

Chloroxylenol 0.3%

Purpose

Antibacterial

Use

 for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product

Stop use and ask a doctor if

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

water, sodium C14-16 olefin sulfonate, lauramine oxide or lauramidopropylamine oxide and myristamidopropylamine oxide, sodium laureth sulfate, sodium lauryl sulfate, sodium chloride, sodium xylenesulfonate, alcohol denat., fragrance, phenoxyethanol, citric acid, methylisothiazolinone, tetrasodium EDTA, yellow 5, blue 1

For more ingredient information, visit CVS.com or call 1-800-SHOP CVS.

Distributed by: CVS Pharmacy, Inc., One CVS Drive,

Woonsocket, RI 02895 (c) 2021 CVS/pharmacy

CVS.com   1-800-SHOP CVS   V-36817

CVS Quality Money Back Guarantee

DSP-TN-21091  DSP-MO-20087

Principal display panel

COMPARE TO DAWN ULTRA ANTIBACTERIAL HAND SOAP*

Total

Home

Antibacterial HAND SOAP

GREEN APPLE

Ultra Concentrated

Tough on Grease

Phosphate-Free Formula

40 FL OZ (1.18 L)

image description

CHLOROXYLENOL 0.3% 
chloroxylenol 0.3% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-946
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL3.0 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
ALCOHOL (UNII: 3K9958V90M)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
EDETATE SODIUM (UNII: MP1J8420LU)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-946-571183 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product01/17/2017
2NDC:69842-946-381123 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product01/17/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/17/2017
Labeler - CVS Pharmacy (062312574)
Registrant - Vi-Jon, LLC (088520668)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(69842-946)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(69842-946)

Revised: 4/2023
Document Id: e0caa2d1-1c4f-4273-8a8c-27fcb691eca5
Set id: 15816a8c-5d76-40b7-a045-c0bbdd62475a
Version: 6
Effective Time: 20230420
 
CVS Pharmacy