NUVALU HAND SANITIZER SWEET PEA BLUE 1OZ by JC SALES / Ningbo Liyuan Daily Chemical Products Co., Ltd.

NUVALU HAND SANITIZER SWEET PEA BLUE 1OZ by

Drug Labeling and Warnings

NUVALU HAND SANITIZER SWEET PEA BLUE 1OZ by is a Otc medication manufactured, distributed, or labeled by JC SALES, Ningbo Liyuan Daily Chemical Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NUVALU HAND SANITIZER SWEET PEA BLUE 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 eys. 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 (aqua), carbomer, fragrance, glycerin, propylene glycol, triethanolamine, tocopheryl acetate (vitamin E), aloe barbadensis leaf juice, FD&C Blue No.1

NUVALU HAND SANITIZER SWEET PEA BLUE 1OZ 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72520-117
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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72520-117-48	29 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

Labeler - JC SALES (610969578)

Registrant - JC SALES (610969578)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Liyuan Daily Chemical Products Co., Ltd.		530766098	manufacture(72520-117)

Revised: 3/2021

Document Id: bd4f7b5e-1a8d-46c3-e053-2995a90a2767

34390-5

Set id: a8d0f1c3-f7f4-516a-e053-2a95a90aa6dd

Version: 3

Effective Time: 20210311