SANTIZALL HAND SANITIZER- ethyl alcohol gel

SANTIZALL HAND SANITIZER by

Drug Labeling and Warnings

SANTIZALL HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by DIVERSIFIED MANUFACTURING CORP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ETHYL ALCOHOL 62% V/V

PURPOSE

ANTISEPTIC

USES

• HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN

WARNINGS

FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.

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 DOCTOR IF IRRITATION OR RASH APPEARS AND LASTS.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

• PUT ENOUGH PRODUCT IN YOUR PALM TO COVER HANDS AND RUB TOGETHER BRISKLY UNTIL DRY
• CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED WHEN USING

OTHER INFORMATION

• STORE BELOW 110°F (43°C)
• MAY DISCOLOR CERTAIN FABRICS OR SURFACES

INACTIVE INGREDIENTS

WATER, GLYCERIN, CARBOMER, TRIETHANOLAMINE, VITAMIN E, ALOE VERA, FRAGRANCE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SANTIZALL HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62172-117
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62172-117-18	238 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/27/2020
2	NDC: 62172-117-14	118 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package	05/27/2020
3	NDC: 62172-117-16	476 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/27/2020
4	NDC: 62172-117-11	3785 mL in 1 JUG; Type 0: Not a Combination Product	05/27/2020
5	NDC: 62172-117-12	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/27/2020

Labeler - DIVERSIFIED MANUFACTURING CORP (185073996)