ANTI-BACTER HAND SANITIZER 70 ETHYL ALCOHOL RED BERRY- alcohol gel

Anti-Bacter Hand Sanitizer 70 Ethyl Alcohol Red Berry by

Drug Labeling and Warnings

Anti-Bacter Hand Sanitizer 70 Ethyl Alcohol Red Berry by is a Otc medication manufactured, distributed, or labeled by ADEX COSMETICS & PHARMA LESZEK SIERDZINSKI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl alcohol 70% v/v

Purpose

Antiseptic

Uses

• for travel, shopping, school, work and home use
• to help reduce bacteria on the skin
• for use when water and soap are not available
• recommended for repeated uses

Warnings:

For external use only: hands

• flammable, keep away from sources of heat or fire

do not use

• on broken, cut or irritated skin

When using this product

keep out of reach of children.

• avoid contact with eyes. if contact occurs, rinse thoroughly with water,

stop using and ak a doctor 

if irritation or redness develops or lasts

• if swallowed, get medical help or contact a Poison Control Center immediately

Directions

• place enough gel in your palms to thoroughly cover hand, rub hands together brikly until dry
• children under 6 years of age should be supervised when using Anti-Bacter Hand Sanitizer
• not recommended for infants

Other information

• store at a temperature below 104°F (40°C)
• may discolor certain fabrics and surfaces

Inactive Ingredients:

AQUA (WATER), GLYCERIN, ALOE BARBADENSIS LEAF JUICE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER / CARBOMER*, MANNITOL, MICROCRYSTALLINE CELLULOSE, HYDROXYPROPYL METHYLCELLULOSE, ALOE BARBADENSIS LEAF JUICE POWDER, TOCOPHERYL ACETATE, ALGIN, PARFUM (FRAGRANCE), AMINOMETHYL PROPANOL, BENZOPHENONE-3, POTASSIUM SORBATE, SODIUM BENZOATE, CI 74260, CI 77492 (IRON OXIDES), CI 17200 (D&C RED 33).
*The letter next to the batch number means:
A-ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER B-CARBOMER

Package Labeling:

INGREDIENTS AND APPEARANCE

ANTI-BACTER HAND SANITIZER 70 ETHYL ALCOHOL RED BERRY 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80457-008
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SODIUM ALGINATE (UNII: C269C4G2ZQ)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
OXYBENZONE (UNII: 95OOS7VE0Y)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80457-008-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2021

Labeler - ADEX COSMETICS & PHARMA LESZEK SIERDZINSKI (366050458)