NURINSE HAND SANITIZER- ethyl alcohol liquid

NuRinse Hand Sanitizer by

Drug Labeling and Warnings

NuRinse Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by NuGenTec. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients:

Ethanol Alcohol 70% v/v,

PURPOSE

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.

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

NURINSE HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77368-070
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
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77368-070-08	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/03/2020
2	NDC: 77368-070-12	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/03/2020
3	NDC: 77368-070-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/03/2020
4	NDC: 77368-070-10	3800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/03/2020

Labeler - NuGenTec (090331927)

Establishment
Name	Address	ID/FEI	Business Operations
NuGenTec		090331927	manufacture(77368-070)