FDA.reportPublic FDA data

NBGS Hand Sanitizer

Manufacturer
National Bio Green Sciences Limited Liability Company
Effective date
2020-04-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:26

Label at a glance#

ProductNBGS Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

Pump a small amount of foam onto hands. Rub thoroughly over surface of both hands. Rub hands together until dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial*

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush out with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

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

  • Pump a small amount of foam onto hands.
  • Rub thoroughly over surface of both hands.
  • Rub hands together until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropylamine Oxide, Cocamidopropyl Hydroxysultaine, Glycereth-2 Cocoate, Cocamidopropyl Betaine, Cetrimonium Chloride.

OTC - QUESTIONS SECTION

Questions:  1-800-223-1467

SPL UNCLASSIFIED SECTION

Antibacterial Foaming

  • Alcohol-Free
  • Powerful & Long Lasting
  • Safe & Soft for Skin
  • pH Neutral

*Kills 99.9% of common, harmful germs in just 15 seconds.

Manufactured by: NATIONAL BIO GREEN SCIENCES LLC (NBGS)

6-b Culnen Dr., Branchburg, NJ, USA 08876

nbgsusa.com

info@nbgsusa.com

NOT TESTED ON ANIMALS

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

nbgsnwnbgsnw

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72678-032-012022-01-28C16284748780-1d6a99b39-a501-a426-e053-dadaa90af4c2NBGS Hand Sanitizer
72678-032-022022-01-28C16284748780-1d6a99b39-a501-a426-e053-dadaa90af4c2NBGS Hand Sanitizer
72678-032-032022-01-28C16284748780-1d6a99b39-a501-a426-e053-dadaa90af4c2NBGS Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72678-032-01NBGS Hand Sanitizer50 mL in 1 BOTTLESOLUTION501
72678-032-02NBGS Hand Sanitizer250 mL in 1 BOTTLESOLUTION2501
72678-032-03NBGS Hand Sanitizer3785 mL in 1 BOTTLESOLUTION37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72678-032NBGS HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [NATIONAL BIO GREEN SCIENCES LIMITED LIABILITY COMPANY]1Legacy NDC, 3 package rows20200503_a12116bf-0501-4318-b50c-d1bdb45b8e4a.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72678-03272678-032-01, 72678-032-02, 72678-032-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT
GLYCERETH-2 COCOATEJWM00VS7HCIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT

Source Document#

Source XML · Source PDF

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
e79a68e1-7b16-4f0b-ad75-75abf9022e4fa12116bf-0501-4318-b50c-d1bdb45b8e4a2020-04-22WarningsExact identifier
spl id: e79a68e1-7b16-4f0b-ad75-75abf9022e4f
spl set id: a12116bf-0501-4318-b50c-d1bdb45b8e4a

Reported adverse events (FAERS/openFDA)#

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