FDA.reportPublic FDA data

Native Green Foaming Hand Sanitizer

Manufacturer
Native Green | Canberra Corporation
Effective date
2010-04-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:27

Label at a glance#

ProductNative Green Foaming Hand Sanitizer
Active ingredientbenzalkonium chloride
Label structure5 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin

Warning

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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 into palm of hand
  • Rub thoroughly over all surfaces of both hands
  • Rub hands together briskly until dry
INACTIVE INGREDIENT SECTION

Inactive Ingredients Water, dihydroxpropyl PEG-5
linoleammonium chloride, glycereth-2 cocoate, behentrimonium
chloride, dihydroxyethyl cocamine oxide, fragrance

Principal Display Panel – Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NATIVE GREEN
FOAMING HAND SANITIZER
ALCOHOL-FREE – WITH MOISTURIZERS

Cleaner, Greener

SEE SIDE PANEL FOR ADDITIONAL INFORMATION.

Principal Display Panel – Bottle Label
Principal Display Panel – Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN1
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD1
1038799benzalkonium chloride 0.1 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50409-514-422019-10-21C16284748780-1956f9ecf-d29c-621f-e053-dbdaa90a74adDrug Facts
50409-514-822019-10-21C16284748780-1956f9ecf-d29c-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50409-514-42Native Green Foaming Hand Sanitizer50 mL in 1 BOTTLESOLUTION501
50409-514-82Native Green Foaming Hand Sanitizer550 mL in 1 BOTTLESOLUTION5501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50409-514NATIVE GREEN FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [NATIVE GREEN]1Legacy NDC, 2 package rows20100510_75c243a8-242c-4ca1-a983-89f07aec3041.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
benzalkonium chlorideACTIVE INGREDIENTF5UM2KM3W71
benzalkoniumACTIVE MOIETY7N6JUD5X6Y1
behentrimonium chlorideINACTIVE INGREDIENTX7GNG3S47T1
dihydroxyethyl cocamine oxideINACTIVE INGREDIENT8AR51R3BL51
dihydroxypropyl peg-5 linoleammonium chlorideINACTIVE INGREDIENT0Y0NQR2GH11
glycereth-2 cocoateINACTIVE INGREDIENTJWM00VS7HC1
waterINACTIVE INGREDIENT059QF0KO0R1

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
50409-51450409-514-82, 50409-514-42

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
benzalkonium chlorideF5UM2KM3W7ACTIB
water059QF0KO0RIACT
dihydroxypropyl peg-5 linoleammonium chloride0Y0NQR2GH1IACT
glycereth-2 cocoateJWM00VS7HCIACT
behentrimonium chlorideX7GNG3S47TIACT
dihydroxyethyl cocamine oxide8AR51R3BL5IACT

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
86f6b0d9-e0f9-4042-9e9c-62607f7679c675c243a8-242c-4ca1-a983-89f07aec30412010-04-02WarningsExact identifier
spl id: 86f6b0d9-e0f9-4042-9e9c-62607f7679c6
spl set id: 75c243a8-242c-4ca1-a983-89f07aec3041

Reported adverse events (FAERS/openFDA)#

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