BEVERLY GEL HAND SANITIZER- ethyl alcohol gel

Beverly Gel Hand Sanitizer by

Drug Labeling and Warnings

Beverly Gel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Cleanslate Group LLC, Betco Corportation LLC, Betco Corporation LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Acive Ingredient

ethyl Alcohol

inactive ingredients

Water

Carbomer

Dimethicone PEG-8 Laurate

Glycerin

EDETOL

Fragrance

Aloe Barbadensis Leaf Juice

dosage

Place enough product on your palm to thoroughly cover your hands

Rub hands together brisky until dry

indications

Hand sanitizer to reduce microorganisms on 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 flame

When using this product avoid contact with eyes.

Stop use and ask doctor if irritaiton or rash occurs.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BEVERLY GEL HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80586-801
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE PEG-8 LAURATE (UNII: 72MF9C2A18)	0.013 mL  in 1 mL
EDETOL (UNII: Q4R969U9FR)	0.0035 mL  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	1 mL  in 1 mL
FRAGRANCE LEMON ORC2001060 (UNII: K1725A7G95)	0.0003 mL  in 1 mL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)	0.0035 mL  in 1 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.00001 mL  in 1 mL
WATER (UNII: 059QF0KO0R)	0.3 mL  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80586-801-04	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/10/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/10/2024

Labeler - Cleanslate Group LLC (117657934)

Registrant - Betco Corportation LLC (005050158)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation LLC		005050158	manufacture(80586-801)