ADVANCED ALCOHOL FOAMING HAND SANITIZER- ethyl alcohol liquid

Advanced Alcohol Foaming Hand Sanitizer by

Drug Labeling and Warnings

Advanced Alcohol Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Betco Corporation LLC, Betco Coporation LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethjyl Alcohol

inactives

Aloe Barbadensis Leaf Juice, D&C Green #5, PEG 10 Perfluorohexylethyl acrylate copolymer, Perluorohexylethyl alcohol, propylene glycol, water

dosage

Please read entire label before using thsi product. Place enough product on your palm to tnoroughly cover your hands, Rub hands together briskyl until dry.

usage

Hand sanitizer to reduce mocroorganisms on the skin.. Use this product when soap and water are not available.

purpose

Antiseptic

keep out of reach

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

warnings

For external use only. FLAMMABLE. This product contains ethyl alcohol. Keep away from heat or flame.

When using this product avoid contact with eyes. If contact occurs rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs.

package label

INGREDIENTS AND APPEARANCE

ADVANCED ALCOHOL FOAMING HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65601-802
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.6787 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	0.2926 mL  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.25 mL  in 1 mL
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)	0.000002 mL  in 1 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.001 mL  in 1 mL
PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER (UNII: D76Z87928N)	0.5 mL  in 1 mL
2-(PERFLUOROHEXYL)ETHANETHIOL (UNII: 66E2ZQ1P07)	0.5 mL  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65601-802-04	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/29/2023
2	NDC: 65601-802-29	1000 mL in 1 BAG; Type 0: Not a Combination Product	12/29/2023
3	NDC: 65601-802-55	208175 mL in 1 DRUM; Type 0: Not a Combination Product	12/29/2023
4	NDC: 65601-802-88	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/11/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/29/2023

Labeler - Betco Corporation LLC (005050158)

Registrant - Betco Coporation LLC (005050158)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation LLC		005050158	manufacture(65601-802)