NURINSE HAND SANITIZER- ethyl alcohol liquid 
NuGenTec

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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NuRinse​® Hand Sanitizer

Active Ingredients:

Ethanol Alcohol 70% v/v,

Purpose: Antiseptic

Use: For external use only on hands.

Inactive Ingredients:

Glycerin (for moisturizing), Hydrogen Peroxide, Water

Directions:

When using NuRinse Hand Sanitizer, apply a palmful of the product to one hand and rub the product all over the surfaces of both hands until your hands are dry. Do not wipe away excess sanitizer. For children under 6, use only with adult supervision. Not recommended for infants.

WARNINGS:​

Flammable: Keep away from heat and flame. Keep container closed when not in use.
When using this product: Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.
Stop use and ask a Doctor: If skin irritation develops.

Keep out of reach of children: If ingested, get medical help or call the Poison Control Center immediately.

Other Information:

Do not store above 105°F. May discolor some fabrics. Harmful to wood finishes and plastics.

World Health Organization Recommended Hand Rub Formulation
*Ethanol 70%

​Advanced Formula
Hand Moisturizing
Hospital & Institutional Grade

Personal Care
Hand Sanitizer
Designed in The USA. Made in The USA.™

Product Description:
Personal care product. Use for hand sanitizing. Recommended for repeated use. The formula contains 70% alcohol (ethanol) which meets the CDC, FDA, and WHO guidelines for hand sanitizer. All USP ingredients. Enhanced WHO formula to increase moisturizing effect.

California Prop 65 Compliant

​Manufactured and Distributed By:

NuGenTec​®

Redefining Chemistry

1155 Park Avenue
Emeryville, CA 94608
Phone (888) 996-8436
salesteam@nugentec.com
www.nugentec.com

Packaging

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NURINSE HAND SANITIZER 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77368-070
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77368-070-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/03/2020
2NDC:77368-070-12355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/03/2020
3NDC:77368-070-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/03/2020
4NDC:77368-070-103800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/03/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/03/2020
Labeler - NuGenTec (090331927)
Establishment
NameAddressID/FEIBusiness Operations
NuGenTec090331927manufacture(77368-070)

Revised: 9/2020
Document Id: 0f20369e-b8b8-45f6-a6cb-49375fb66543
Set id: eff89b44-44c1-4f2f-a5ce-0093cbad805c
Version: 1
Effective Time: 20200903
 
NuGenTec