CHLOROXYLENOL 0.3% liquid

Chloroxylenol 0.3% by

Drug Labeling and Warnings

Chloroxylenol 0.3% by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

• do not get into eyes.  If contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

• irritation or redness develops
• condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

• wet hands
• apply palmful to hands
• scrub thoroughly
• rinse thoroughly

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

SPL UNCLASSIFIED SECTION

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)

INGREDIENTS AND APPEARANCE

CHLOROXYLENOL 0.3% 
chloroxylenol 0.3% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-946
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-946-57	1183 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	01/17/2017
2	NDC: 69842-946-38	1123 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	01/17/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/17/2017

Labeler - CVS Pharmacy (062312574)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(69842-946)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(69842-946)