FDA.reportPublic FDA data

Greenberry

Manufacturer
Greenberry Eco Group LLC
Effective date
2020-06-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:16:46

Label at a glance#

ProductGreenberry
Active ingredientBenzalkonium Chloride
Label structure8 sections

Indications and uses

Decreases bacteria on skin.

Dosage and administration

Open lid and remove wipes. Wet hands thoroughly with product and let hands air dry. Throw used wipe in trash. Do not flush.  Adults and children 2 years and over:  Apply to hands. allow hands to dry without wiping.  Children under 2 years:  Ask a doctor before use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial agent

Uses

INDICATIONS & USAGE SECTION

Decreases bacteria on skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use if you are allergic to any of the ingredients.

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash develops and continues 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

Open lid and remove wipes.
Wet hands thoroughly with product and let hands air dry.
Throw used wipe in trash.
Do not flush.

 Adults and children 2 years and over: Apply to hands. allow hands to dry without wiping.
 Children under 2 years: Ask a doctor before use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

c12-14 Alkyl Dymethyl, Ethylbenzyl Ammonium Chloride, Alkyl Polyglucoside, Disodium EDTA, Propylene glycol, Aqua

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label, 10 Wipes

Label_1Label_1

Label 110 Wipes
Label_2Label_2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77965-001-012023-01-30C16284748780-1f386c649-9dd5-0266-e053-dadaa90a7c1a013fd60f-e7f0-4098-b2f8-9e75c7fcc765
77965-001-022023-01-30C16284748780-1f386c649-9dd5-0266-e053-dadaa90a7c1a013fd60f-e7f0-4098-b2f8-9e75c7fcc765
77965-001-032023-01-30C16284748780-1f386c649-9dd5-0266-e053-dadaa90a7c1a013fd60f-e7f0-4098-b2f8-9e75c7fcc765

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
77965-00177965-001-01, 77965-001-02, 77965-001-03

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
N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM (C12-C14)85440928RVIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT

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
464fc0e5-8f9e-4882-a476-33cd38b3dbd7013fd60f-e7f0-4098-b2f8-9e75c7fcc7652020-06-09WarningsExact identifier
spl id: 464fc0e5-8f9e-4882-a476-33cd38b3dbd7
spl set id: 013fd60f-e7f0-4098-b2f8-9e75c7fcc765

Reported adverse events (FAERS/openFDA)#

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