NuRinse Hand Sanitizer-Q

Manufacturer
NuGenTec
Effective date
2022-12-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:52:37

Label at a glance#

ProductNuRinse Hand Sanitizer-Q
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

When using NuRinse Hand Sanitizer-Q, 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

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F) Do not store above 120°F. May discolor some fabrics. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer, Antibacterial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

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.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • When using NuRinse Hand Sanitizer-Q, 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.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)
  • Do not store above 120°F.
  • May discolor some fabrics.
  • Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

  • Purified water USP
  • Humectant
  • Moisturizer
  • Foaming agent

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

750mL is one bottle NDC: 77368-901-75 NuRinse Q LabelNuRinse Q Label

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77368-903-01NuRinse Hand Sanitizer-Q3786 mL in 1 BOTTLELIQUID37863
77368-903-02NuRinse Hand Sanitizer-Q60 mL in 1 BOTTLE, SPRAYLIQUID603
77368-903-05NuRinse Hand Sanitizer-Q18927 mL in 1 BOTTLELIQUID189273
77368-903-10NuRinse Hand Sanitizer-Q1000 mL in 1 BOTTLELIQUID10003
77368-903-75NuRinse Hand Sanitizer-Q750 mL in 1 BOTTLE, SPRAYLIQUID7503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77368-903NURINSE HAND SANITIZER-Q (BENZALKONIUM CHLORIDE) LIQUID [NUGENTEC]3Legacy NDC, 5 package rows20221223_f0744946-28d8-7977-e053-2a95a90a69a5.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77368-90377368-903-75, 77368-903-02, 77368-903-10, 77368-903-05, 77368-903-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
f0745db0-dfe8-3793-e053-2995a90a2954f0744946-28d8-7977-e053-2a95a90a69a52022-12-22WarningsExact identifier
spl id: f0745db0-dfe8-3793-e053-2995a90a2954
spl set id: f0744946-28d8-7977-e053-2a95a90a69a5

Reported adverse events (FAERS/openFDA)#

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