SIMPLIFY ANTIBACTERIAL HAND ORANGE SCENT- chloroxylenol soap

Simplify Antibacterial Hand by

Drug Labeling and Warnings

Simplify Antibacterial Hand by is a Otc medication manufactured, distributed, or labeled by Zhejiang Qimei Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Chloroxylenol 0.30%

Purpose

Antibacterial hand soap

Use

For handwashing to decrease bacteria on the skin

Warnings

For external use only

KEEP OUT OF REACH OF CHILDREN.

May cause moderate eye irritation. Avoid contact with eyes and skin. If in eyes, flush eyes gently with water for 15 minutes. If swallowed, drink water to dilute. If irritation persists, contact a Physician or Poison Control Center.

Directions

• Wet hands.
• Apply palmful to hands.
• Scrub thoroughly and rinse with water.

Inactive Ingredients

Carbamide, citric acid, cocamidopropyl betaine, DMDM hydroton, dodecylbenzene sulfonic acid, ethyl alcohol, fragrance, lauramine oxide, sodium chloride, sodium hydroxide, sodium lauryl ether sulfate, sodium xylene sulfonate, water

19.4 FL OZ (1.21 PT) 573 mL

Compare to

Dawn ® Ultra Antibacterial

Simplify ®

Antimicrobial

Hand Soap & Ultra Dish

Detergent

• Contains no

phosphates

• Cuts Grease

ORANGE

SCENT

19.4 FL OZ (1.21 PT) 573 mL

INGREDIENTS AND APPEARANCE

SIMPLIFY ANTIBACTERIAL HAND  ORANGE SCENT
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81773-014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
DODECYLBENZENESULFONIC ACID (UNII: 60NSK897G9)
WATER (UNII: 059QF0KO0R)
UREA (UNII: 8W8T17847W)
SODIUM C12-14 ALKETH-3 SULFATE (UNII: 5G80BO01PI)
ALCOHOL (UNII: 3K9958V90M)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
DMDM HYDANTOIN (UNII: BYR0546TOW)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81773-014-01	573 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/09/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/09/2023

Labeler - Zhejiang Qimei Cosmetics Co., Ltd. (709887693)