NOVO FOAMING INSTANT HAND SANITIZER- ethyl alcohol liquid

Novo Foaming Instant Hand Sanitizer by

Drug Labeling and Warnings

Novo Foaming Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Noble Chemical Inc., Betco Corporation LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

active ingredient

Ethyl Alcohol 70% V/V

Inactive ingredient

Aloe Barbadensis leaf Juice, D&C Green #5, Fragrance, PEG-10 acrylate/perfluorohextl acrylate copolymer, Perfluorohexylethyl alcohol, Propylene Glycol, Water

dosage

Apply liberally to hands to cover all surfaces

Rub hands together until dry

Supervise children under 6 years old

Not recommended for infants

Indications

To decrease bacteria on hands when changing diapers,assiting ill persons or before contact with a person under medical care or treatment

Recommended for repeated use

Use this product when soap and water are not available

puepose

Antiseptic

Keep out of Reach

Keep out of reach of children. If swallowed get medical help or contact poison control center immediately.

warnings

For external use only

Flammable, keep away from fire or flame

When using product avoid contact with eyes. In case of eye contact, rinse eyes with water

Stop use and ask doctor if irritation or redness develop or last more than 72 hours

label

INGREDIENTS AND APPEARANCE

NOVO FOAMING INSTANT HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81551-802
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)	0.0113 mL  in 1 mL
WATER (UNII: 059QF0KO0R)	0.27 mL  in 1 mL
EDETOL (UNII: Q4R969U9FR)	0.0035 mL  in 1 mL
FRAGRANCE LEMON ORC2001060 (UNII: K1725A7G95)	0.0003 mL  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.00113 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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81551-802-04	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/16/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/16/2024

Labeler - Noble Chemical Inc. (054146402)

Registrant - Betco Corporation LLC (005050158)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation LLC		005050158	manufacture(81551-802)