NuRinse Hand Sanitizer

Manufacturer
NuGenTec
Effective date
2020-09-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:28:44

Label at a glance#

ProductNuRinse Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

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.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Ethanol Alcohol 70% v/v,

OTC - PURPOSE SECTION

Purpose: Antiseptic

INDICATIONS & USAGE SECTION

Use: For external use only on hands.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Glycerin (for moisturizing), Hydrogen Peroxide, Water

Directions:

DOSAGE & ADMINISTRATION SECTION

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:​

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Other Information:

STORAGE AND HANDLING SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

PackagingPackaging

PackagingPackaging

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77368-070-08NuRinse Hand Sanitizer236 mL in 1 BOTTLE, PLASTICLIQUID2361
77368-070-10NuRinse Hand Sanitizer3800 mL in 1 BOTTLE, PLASTICLIQUID38001
77368-070-12NuRinse Hand Sanitizer355 mL in 1 BOTTLE, PLASTICLIQUID3551
77368-070-16NuRinse Hand Sanitizer473 mL in 1 BOTTLE, PLASTICLIQUID4731

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77368-070NURINSE HAND SANITIZER (ETHYL ALCOHOL) LIQUID [NUGENTEC]1Legacy NDC, 4 package rows20200908_eff89b44-44c1-4f2f-a5ce-0093cbad805c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77368-07077368-070-08, 77368-070-12, 77368-070-16, 77368-070-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0f20369e-b8b8-45f6-a6cb-49375fb66543eff89b44-44c1-4f2f-a5ce-0093cbad805c2020-09-03WarningsExact identifier
spl id: 0f20369e-b8b8-45f6-a6cb-49375fb66543
spl set id: eff89b44-44c1-4f2f-a5ce-0093cbad805c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.