SAFEGUARD ANTIBACTERIAL HAND- chloroxylenol liquid

Safeguard Antibacterial Hand by

Drug Labeling and Warnings

Safeguard Antibacterial Hand by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Chloroxylenol 0.5%

Purpose

Antibacterial

Use

• For handwashing to decrease bacteria on skin. Recommended for repeated use.

Warnings

For external use only.

Do not use this product on infants under 6 months of age.

When using this product avoid contact with eyes. If this happens, rinse thoroughly with water.

Stop use if irritation occurs.

Keep out of reach of children, except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet hands and forearms. Apply 5 milliliters (teaspoonful) or palmful to hands and forearms. Scrub thoroughly for 20 seconds and rinse.

Inactive ingredients

water, sodium lauryl sulfate, sodium laureth sulfate, lauramide DEA, glycol distearate, cocamidopropyl betaine, sodium sulfate, fragrance, citric acid, guar hydroxypropyltrimonium chloride, DMDM hydantoin, tetrasodium EDTA, yellow 5, red 4

Questions?

1-800-332-7787

SPL UNCLASSIFIED SECTION

Distr. by PROCTER & GAMBLE, CINCINNATI, OH 45202.

PRINCIPAL DISPLAY PANEL - 3.78 L Bottle Label

Liquid Ready-to-Use

Safeguard™ Antibacterial Hand Soap

• Helps remove bacteria
  from skin

Chloroxylenol Antibacterial Hand Soap

DATA RATES APPLY

2-10

P&G
Professional ™
3.78 L/1 GALLON

INGREDIENTS AND APPEARANCE

SAFEGUARD ANTIBACTERIAL HAND 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-053
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM SULFATE (UNII: 0YPR65R21J)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DMDM HYDANTOIN (UNII: BYR0546TOW)
EDETATE SODIUM (UNII: MP1J8420LU)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-053-37	3780 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/01/2015
2	NDC: 69423-053-80	800 mL in 1 POUCH; Type 0: Not a Combination Product	11/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/01/2015

Labeler - The Procter & Gamble Manufacturing Company (004238200)