NuValu® ADVANCED HAND SANITIZER

NUVALU ADVANCED HAND SANITIZER by

Drug Labeling and Warnings

NUVALU ADVANCED HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by J C SALES. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NUVALU ADVANCED HAND SANITIZER- alcohol gel 
J C SALES

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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NuValu® ADVANCED HAND SANITIZER

Drug Facts

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Inactive Ingredients:

Water, Aloe Barbadensis Leaf Extract, Carbomer, Parfum, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine, FD&C Yellow No.5, Tartrazine, FD&C Blue No.1

Warning

Flammable. Keep away from fire or flame.

For external use only.

When using this 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.

Use:

NuValu Advanced Hand Sanitizer helps reduce bacteria and moisturizes skin.

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 by adult when using this product.

Other Information

• Store below 100°F (38°C)
• May discolor certain fabrics or surfaces.

KILLS GERMS

• Contains vitamin E
• Moisturizes hands

Distributed by JC Sales, Los Angeles, CA 90058

Made in China

Packaging

NUVALU ADVANCED HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72520-003
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
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72520-003-12	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/25/2020	05/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/25/2020	05/01/2022

Labeler - J C SALES (610969578)

Revised: 7/2022

Document Id: 22477093-6738-4cbe-8737-258e01598b47

34390-5

Set id: 0dd2d197-3370-43cf-b614-b7b3d153ba28

Version: 2

Effective Time: 20220711