NUVALU HAND SANITIZER GUAVA BURST 1OZ- ethyl alcohol gel
JC 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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Drug Facts
Active Ingredient

Ethyl Alcohol 70 percent

Purpose

Antimicrobial

Features

To decrease bacteria on the skin that could cause disease.
Recommended for repeated use.
Use anywhere without water.

Directions

Wet hands thoroughly with product and rub until dry without wiping.
For children under 6, use only under adult supervision.
Not recommended for infants.

When using this product

Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Do not inhale or ingest.
Avoid contact with broken skin.

Other information

Do not store above 105 Fahrenheit
May discolor some fabrics
Harmful to wood finishes and plastics

Warnings

For external use only.
Flammable. Keep away from heat and flame.
Discontinue if skin becomes irritated and ask a doctor.

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Inactive Ingredients

Water, Carbomer, Fragrance, Glycerin, Propylene Glycol, Triethanolamine, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, FD&C Red No.40, FD&C Yellow No.5

label

NUVALU HAND SANITIZER GUAVA BURST 1OZ
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:72520-118
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
FD&C RED NO. 40 (UNII: WZB9127XOA)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
CARBOMER 934 (UNII: Z135WT9208)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72520-118-48	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/01/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	03/01/2021

Labeler - JC SALES (610969578)

Registrant - JC SALES (610969578)

Name	Address	ID/FEI	Business Operations
Establishment
Ningbo Liyuan Daily Chemical Products Co., Ltd.		530766098	manufacture(72520-118)

Drug Facts Active Ingredient