WILLIAMS HAND SANITIZER- alcohol spray

Williams Hand Sanitizer by

Drug Labeling and Warnings

Williams Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Combe Incorporated. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Williams Hand Sanitizer Spray

Drug Facts

Active ingredient

Ethyl Alcohol 70% w/w

Purpose

Antimicrobial

Use

to help reduce bacteria on the skin. For use when soap and water are not available.

Warnings

Flammable. Keep away from fire or flame.

For external use only.

When using this product,

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. 

Stop use and ask a doctor

if irritation or rash appears. Do not use on broken skin.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Spray enough products on hands to cover all surfaces. Rub hands together briskly until dry.
  
• Rub hands together briskly until dry.
  
• Children should be supervised when using this product.

Other Information

• Store below 86°F (30°C)
  
• May discolor certain fabrics or surfaces

Questions?

Call 1-800-431-2610 weekdays 9 am to 5 pm EST

Inactive ingredients

water, glycerin, aloe barbadensis leaf juice powder.

PRINCIPAL DISPLAY PANEL

Williams

Hand Sanitizer Spray

Kills 99.9% of many common bacteria

Active Antibacterial Ingredient: 70% Alcohol

Moisturizing Glycerin + Aloe

Fragrance Free

1 fl. oz. (29.5 mL)

INGREDIENTS AND APPEARANCE

WILLIAMS HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11509-0401
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11509-0401-1	29.5 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	05/18/2020

Labeler - Combe Incorporated (002406502)