CWGC (as PLD) - DELICARE ANTIBACTERIAL HAND SOAP (70415-502) - DELIST

DELICARE ANTIBACTERIAL HAND by

Drug Labeling and Warnings

DELICARE ANTIBACTERIAL HAND by is a Otc medication manufactured, distributed, or labeled by CWGC LA Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DELICARE ANTIBACTERIAL HAND- chloroxylenol soap 
CWGC LA Inc.

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CWGC (as PLD) - DELICARE ANTIBACTERIAL HAND SOAP (70415-502) - DELIST

Active ingredient

Chloroxylenol, 0.5%

Purpose

Antibacterial

PURPOSE

ANTIBACTERIAL

USES

• For handwashing to reduce bacteria on the skin

WARNINGS

For external use only

When using this product

• Avoid contact with eyes. In case of eye contact, flush with water

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center rihgt away.

DIRECTIONS

• Apply foaming cleanser to dry hands
• Rub hands together to spread lather
• Wash for 15-20 seconds
• Rinse & dry hands thoroughly

Inactive ingredients

Water, Sodium Laureth Sulfate, Isopropyl Alcohol, Cocamidopropyl Betaine, Decyl Glucoside, SODIUM C14-16 OLEFIN SULFONATE, Hydrogenated castor Oil, DMDM Hydantoin, Citric Acid, Fragrance, FD&C Blue No.1, FD&C Yellow No.5.

DELICARE ANTIBACTERIAL HAND 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70415-502
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
DMDM HYDANTOIN (UNII: BYR0546TOW)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70415-502-01	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/21/2020	12/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/21/2020	12/31/2022

Labeler - CWGC LA Inc. (034967904)

Revised: 9/2023

Document Id: 05df9026-0400-1813-e063-6394a90a81da

34390-5

Set id: 73be3606-84d1-48d1-a241-9916c06b43f5

Version: 5

Effective Time: 20230921

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