SANTOTIZER- hand santizer solution liquid

Santotizer by

Drug Labeling and Warnings

Santotizer by is a Otc medication manufactured, distributed, or labeled by Santolubes LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Alcohol 80% v/v

DOSAGE & ADMINISTRATION

WARNINGS

INACTIVE INGREDIENT

INDICATIONS & USAGE

KEEP OUT OF REACH OF CHILDREN

PURPOSE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SANTOTIZER 
hand santizer solution liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73976-1330
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.125 L  in 100 L
WATER (UNII: 059QF0KO0R)	18.4 L  in 100 L
GLYCERIN (UNII: PDC6A3C0OX)	1.45 L  in 100 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73976-1330-3	200 L in 1 DRUM; Type 0: Not a Combination Product	03/30/2020
2	NDC: 73976-1330-1	3.6 L in 1 PAIL; Type 0: Not a Combination Product	03/30/2020
3	NDC: 73976-1330-2	18 L in 1 PAIL; Type 0: Not a Combination Product	03/30/2020
4	NDC: 73976-1330-4	1022 L in 1 TANK; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - Santolubes LLC (144734980)

Registrant - Santolubes LLC (144734980)

Establishment
Name	Address	ID/FEI	Business Operations
Santolubes LLC		144734980	manufacture(73976-1330)