NUVALU INSTANT HAND SANITIZER ALOE VERA- ethyl alcohol gel

NUVALU INSTANT HAND SANITIZER ALOE VERA by

Drug Labeling and Warnings

NUVALU INSTANT HAND SANITIZER ALOE VERA by is a Otc medication manufactured, distributed, or labeled by Ningbo Liyuan Daily Chemical Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INSTANT HAND SANITIZER

helps fight germs without needing to wash your hands

Take it with you when you are on the go

Fight germs, anywhere, anytime.

Use anyplace:

Home

School

Work

Outdoors

Carry in:

Purse

Pocket

Briefcase

Backpack

Glove box

Drug Facts Active Ingredient

Ethyl Alcohol 70 percent

Purpose

Antimicrobial

Uses

Helps reduce bacteria on the skin.

Warnings

Flammable. Keep away from hear or flame.

For external use only.

When using the product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor if

irritation or rash appears and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry.
• Children under 6 years of age should be supervised when using the product.

Other information

• Store below 106 Fahrenheit (41 Degree Celsius)
• May discolor certain fabrics or surfaces.

Inactive Ingredients:

water (aqua), carbomer, fragrance, glycerin, propylene glycol, triethanolamine, tocophereyl acetate (vitamin E), aloe barbadensis leaf juice, FD&C Yellow No.5, FD&C Blue No.1

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NUVALU INSTANT HAND SANITIZER ALOE VERA 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76176-211
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
CARBOMER 934 (UNII: Z135WT9208)
GLYCERIN (UNII: PDC6A3C0OX)
CUPRIC BIS(TRIETHANOLAMINE) (UNII: YBM44X0B6H)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76176-211-36	120 mL in 1 BLISTER PACK; Type 0: Not a Combination Product	11/01/2018
2	NDC: 76176-211-01	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/01/2018

Labeler - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)

Registrant - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Liyuan Daily Chemical Products Co., Ltd.		530766098	manufacture(76176-211)