GERMS BE GONE HAND SANITIZER- alcohol liquid

Germs be gone hand Sanitizer by

Drug Labeling and Warnings

Germs be gone hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Brands International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Ethyl Alcohol, 75% v/v

Purpose

Antiseptic (skin) clenser

Uses

• Antiseptic (skin) clenser

Warnings

For external use only. Flammable, keep away from fire or flame.

When using this product keep out of eyes. Avoid contact with eyes. If contact with eyes occurs, rinse  thoroughly with water.

Stop use and ask a doctor if   irritation develops.

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

Directions

• For occasional and personal domestic use.
• Rub thoroughly into hands for at least 30 secoand Allow to dry.
• Supervise children in the use of this product.

Other Information

• Store below 43°C (110°F)
• may discolor certain fabrics or surfaces

Inactive Ingredients

carbomer, aloe barbadensis leaf juice, aminomethyl propanol, glycerin, propylene glycol, water, isopropyl myristate, tocopheryl acetate (Vit E).

Please see label on the container.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GERMS BE GONE HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-520
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-520-59	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/03/2020

Labeler - Brands International (243748238)

Registrant - Brands International (243748238)

Establishment
Name	Address	ID/FEI	Business Operations
Brands International		243748238	manufacture(50157-520)