Active ingredient

Chloroxylenol 0.5%

Purpose

Antiseptic Handwash

Uses

For handwashing to decrease bacteria on the skin.

Warnings

For external use only

Do not use

In eyes

When using this product

If in eyes, rinse promptly and thoroughly with water
Discontinue use if irritation and redness develop

Stop use and ask a doctor if

Skin irritation or redness occurs 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 and forearms • Apply palmful to hands and forearms.
Scrub thoroughly • Rinse and dry.

Other Information

for additional information, see Safety Data Sheet (SDS)
Medical Emergency: (800) 391-1504

Inactive ingredients: water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, glycerin, citric acid, coco-glucoside, glyceryl oleate, fragrance, methychloroisothiazolinone, CI 19140 (FD&C Yellow No. 5), methylisothiazolinone, CI 14700 (FDC Red No. 4)

Questions? Call (800) 654-8030

Principal display panel and representative label

Rushing

1110840

Foaming Antibacterial Hand Soap

Foaming Antibacterial Hand Soap is a rich lather hand soap with

a balanced blend of cleaning agents and skin protecting moisturizers.

KEEP OUT OF REACH OF CHILDREN • FOR INSTITUTIONAL USE ONLY

Chloroxylenol 0.5%

To obtain Spanish Instructions, see outer carton.

Net contents: 42 US fl oz (1250 ml) NDC 63146-308-10

Distributed by | Distribuido por:

SSDC · 4050 Corporate Dr., #100

Grapevine, Texas 76051-2326 USA

Customer Service: (800) 654-8030

Made in USA | Hecho en Estados Unidos

774260-00 · RSHGUSA 774260/8000/0918

representative label

RUSHING FAHS
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:63146-308
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	5 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
SODIUM SULFATE (UNII: 0YPR65R21J)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
COCO GLUCOSIDE (UNII: ICS790225B)
GLYCERYL OLEATE (UNII: 4PC054V79P)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:63146-308-10	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/09/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	01/09/2019

Labeler - Kay Chemical Co. (003237021)

Drug Facts