HAND SAN 510- isopropyl alcohol liquid

Hand San 510 by

Drug Labeling and Warnings

Hand San 510 by is a Otc medication manufactured, distributed, or labeled by DuBois Chemicals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Hand San 510 Ingredient

Active ingredient[s] Purpose
Isopropyl alcohol 75% v/v ....................................................................................Antiseptic

Purpose - Use

Use[s]
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

warnings

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

do not use

Do not use
in children less than 2 months of age
on open skin wounds

When using

Stop using

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

Kepp out of Reach

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

Directions for use

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

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

Inactive

Inactive ingredients glycerin, hydrogen peroxide, purified water USP

Indications

Use[s]
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

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.

Principal Display for drum

HAND SAN 510
Topical Solution
Hand Sanitizer
Non-sterile Solution
208.2 L (55 U.S. Gal)

Attached immage contains the entire label content for this package size

INGREDIENTS AND APPEARANCE

HAND SAN 510 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44395-1111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.75 L  in 1 L

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.0145 L  in 1 L
WATER (UNII: 059QF0KO0R)	0.23425 L  in 1 L
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.00125 L  in 1 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44395-1111-2	18.9 L in 1 PAIL; Type 0: Not a Combination Product	03/19/2020
2	NDC: 44395-1111-3	208.2 L in 1 DRUM; Type 0: Not a Combination Product	03/19/2020
3	NDC: 44395-1111-1	3.79 L in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/19/2020

Labeler - DuBois Chemicals, Inc. (828235445)

Registrant - DuBois Chemicals, Inc. (828235445)

Establishment
Name	Address	ID/FEI	Business Operations
DuBois Chemicals, Inc.		828235445	manufacture(44395-1111)