NSUUS HAND SANITIZER- alcohol gel

NSUUS HAND SANITIZER by

Drug Labeling and Warnings

NSUUS HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Rainbow Co Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ethyl alcohol

INACTIVE INGREDIENT

Water, Glycerin, Carbomer, dipropylene glycol, triethaneolamine, peg-60 hydrogenated castor oil, panthenol, camellia sinensis leaf extract, diethanolamine, grapefruit peel oil

PURPOSE

to desrease bacteria on hands.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.

Supervise children in the use of this product.

WARNINGS

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NSUUS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74247-0002
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
PANTHENOL (UNII: WV9CM0O67Z)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIETHANOLAMINE (UNII: AZE05TDV2V)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
GRAPEFRUIT OIL (UNII: YR377U58W9)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CARBOMER 940 (UNII: 4Q93RCW27E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74247-0002-1	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
2	NDC: 74247-0002-2	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
3	NDC: 74247-0002-3	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020
4	NDC: 74247-0002-4	70 mL in 1 TUBE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/01/2020

Labeler - Rainbow Co Ltd (690423720)

Registrant - Rainbow Co Ltd (690423720)

Establishment
Name	Address	ID/FEI	Business Operations
Rainbow Co Ltd		690423720	manufacture(74247-0002)