BAC-SAN- foaming hand sanitizer aerosol, foam

BAC-SAN by

Drug Labeling and Warnings

BAC-SAN by is a Otc medication manufactured, distributed, or labeled by DeVere Company, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient:
Ethyl Alcohol (Ethanol) 70.0%................antiseptic antimicrobial

PURPOSE

ALCOHOL FOAMING HAND SANITIZER
This product is an alcohol-based hand sanitizer designed to produce a light foam and spread evenly. Bac-San meets the US Center for Disease Controls recommendations for broad-spectrum sanitizers for use on hands. Bac-San sanitizes hands and leaves a fresh aloe scent.

INDICATIONS & USAGE

Directions

1. Apply liberally into palm of hand

2. Rub hands together to spread foam evenly

3. Allow hands to air dry

WARNINGS

FIRST AID: IF IN EYES: Rinse cautiously with water for several minutes.

Remove contact lenses, if present and easy to do. Continue rinsing. IF ON SKIN: Wash with plenty of water. IF INHALED: Remove victim to fresh air and keep at rest in a posltion comfortable for breathing. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. 

INACTIVE INGREDIENT

Inactive Ingredients
Water, glycerin, surfactant, aloe

DOSAGE & ADMINISTRATION

Directions

1. Apply liberally into palm of hand

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BAC-SAN 
foaming hand sanitizer aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76315-2020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	1.45 L  in 100 L
WATER (UNII: 059QF0KO0R)	28.52 L  in 100 L
CYCLOMETHICONE 4 (UNII: CZ227117JE)	0.026 L  in 100 L
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.004 L  in 100 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76315-2020-1	3.8 L in 1 JUG; Type 0: Not a Combination Product	08/18/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M	08/16/2022

Labeler - DeVere Company, Inc. (006074579)

Registrant - DeVere Company, Inc. (006074579)

Establishment
Name	Address	ID/FEI	Business Operations
DeVere Company, Inc.		006074579	api manufacture(76315-2020)