NO-GERMS Hand Sanitizer

Manufacturer
Millennium Research USA LLC | Millennium Research Llc
Effective date
2020-07-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:31

Label at a glance#

ProductNO-GERMS Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

Directions Read the entire label before using this product. Apply liberally to the hands and rub together until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic Sanitizer

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to help reduce bacteria on skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Do not spray in the eyes.

  • When using this product, avoid contact with eyes. In case of contact, flush eyes with water.
  • Stop use and ask a doctor if redness or irritation occurs and persist for more than 72 hours
  • KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children should be supervised when using this product.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

Read the entire label before using this product.

Apply liberally to the hands and rub together until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Citric Acid, Matricaria (Chamomilla Recutita) Flower Extract, Lavender (Lavandula Angustifolia) Extract, Aloe Barbadensis Leaf Juice

25 ml NDC 79851-019-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

25 ml label25 ml label

4 L NDC 79851-019-05

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4 L label4 L label

50 ml NDC 79851-019-03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 ml label50 ml label

210 ml NDC 79851-019-09

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

210 ml label210 ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039012benzalkonium chloride 0.13 % Topical SprayPSN1
1039012benzalkonium chloride 1.3 MG/ML Topical SpraySCD1
1039012benzalkonium chloride 0.13 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79851-019-01NO-GERMS Hand Sanitizer25 mL in 1 BOTTLE, SPRAYLIQUID251
79851-019-03NO-GERMS Hand Sanitizer50 mL in 1 BOTTLE, PUMPLIQUID501
79851-019-04NO-GERMS Hand Sanitizer210 mL in 1 BOTTLE, PUMPLIQUID2101
79851-019-05NO-GERMS Hand Sanitizer4000 mL in 1 BOTTLELIQUID40001
79851-019-06NO-GERMS Hand Sanitizer12 in 1 CASELIQUID121
79851-019-07NO-GERMS Hand Sanitizer12 in 1 CASELIQUID121
79851-019-08NO-GERMS Hand Sanitizer24 in 1 CASELIQUID241

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79851-019NO-GERMS HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [MILLENNIUM RESEARCH USA LLC]1Legacy NDC, 7 package rows20200917_aa92fb87-9cda-ee8c-e053-2a95a90a1c30.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
79851-01979851-019-01, 79851-019-07, 79851-019-08, 79851-019-03, 79851-019-06, 79851-019-04, 79851-019-05

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
aa8f2a8a-2167-3291-e053-2a95a90a5798aa92fb87-9cda-ee8c-e053-2a95a90a1c302020-07-16WarningsExact identifier
spl id: aa8f2a8a-2167-3291-e053-2a95a90a5798
spl set id: aa92fb87-9cda-ee8c-e053-2a95a90a1c30

Reported adverse events (FAERS/openFDA)#

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