KILLS HAND SANITIZER- alcohol gel

Kills Hand Sanitizer by

Drug Labeling and Warnings

Kills Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Dermazone Solutions, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient[s]

Ethyl Alcohol, USP 65% v/v

Purpose

Antimicrobial

Use[s]

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15 - 30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Aloe Barbadensis leaf juice

Glycerin, USP

Hydroxypropyl cellulose, NF

Purified Water, USP

SPL UNCLASSIFIED SECTION

Manufactured by:

Dermazone Solutions, Inc.
St. Petersburg, FL 33713

PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label

Kills

Hand Sanitizer

• Antibacterial
  formula.
• Immediately eliminates 99.99%
  of common germs
  and bacteria.
• Made in FDA
  registered
  drug facility.

FDA

8 fl oz (236ml)

INGREDIENTS AND APPEARANCE

KILLS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58466-105
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
aloe vera leaf (UNII: ZY81Z83H0X)
glycerin (UNII: PDC6A3C0OX)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58466-105-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/10/2020
2	NDC: 58466-105-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/10/2020

Labeler - Dermazone Solutions, Inc. (136116865)