TrueLiving 560.002/560AC-AD-AE Antibacterial Hand Soap

Chloroxylenol by

Drug Labeling and Warnings

Chloroxylenol by is a Otc medication manufactured, distributed, or labeled by Old East Main Co, Vi-Jon, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CHLOROXYLENOL- chloroxylenol liquid 
Old East Main Co

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TrueLiving 560.002/560AC-AD-AE
Antibacterial Hand Soap

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 and redness develop
• 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 and/or lauramidopropylamine oxide and myristamidopropylamine oxide, sodium laureth sulfate, sodium lauryl sulfate, sodium chloride, sodium xylenesulfonate, alcohol denat., fragrance, limonene, phenoxyethanol, citric acid, methylisothiazolinone, tetrasodium EDTA, yellow 5, red 33

Do not add bleach.

Not for use in dishwashers.

Contains Surfactants  Phosphate Free

**When compared to non-concentrated formulas

*This product is not manufactured or distributed by Procter & Gamb;le, distributor of Dawn Ultra Antibacterial Hand Soap Orange Scent

principal display panel

ULTRA CONCENTRATED 3X CLEANING POWER

trueliving

ULTRA

Antibacterial

Hand Soap

Dishwashing Liquid

TOUGH ON GREASE

Compare to Dawn Ultra Antibacterial Hand Soap Orange Scent

CITRUS ORANGE SCENT

18 FL OZ (532 mL)

CHLOROXYLENOL 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55910-984
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3.09 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
WATER (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALCOHOL (UNII: 3K9958V90M)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
DITETRACYCLINE TETRASODIUM EDETATE (UNII: WX0A0IT7K5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55910-984-44	532 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	12/01/2020	08/04/2024
2	NDC: 55910-984-57	1183 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	12/01/2020	08/26/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/01/2020	08/26/2024

Labeler - Old East Main Co (068331990)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(55910-984)

Revised: 10/2024

Document Id: 2381308e-99a5-b4c5-e063-6394a90ac687

34390-5

Set id: cb7bc2ad-0794-46be-9457-e50767d7ef70

Version: 8

Effective Time: 20241002