FDA.reportPublic FDA data

GrowDefender Antibacterial Foam

Manufacturer
Grow Defender LLC | AP Goldshield LLC | RWM Technologies, LLC
Effective date
2025-10-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:16:22

Label at a glance#

ProductGrowDefender Antibacterial Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For hand washing to help reduce bacteria on skin that could cause disease.

Dosage and administration

Foam onto palm, massage into hands and under fingernails and air dry. Young children use with supervision.

Storage and handling

At room temperature not below 33°F.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic / Antimicrobial

Uses

INDICATIONS & USAGE SECTION

For hand washing to help reduce bacteria on skin that could cause disease.

Directions

DOSAGE & ADMINISTRATION SECTION

Foam onto palm, massage into hands and under fingernails and air dry. Young children use with supervision.

Store

STORAGE AND HANDLING SECTION

At room temperature not below 33°F.

Other Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Propylene Glycol, Methyl Anthranilate, Trihydroxysilylpropyldimethylocatedecyl Ammonium Chloride.

CAUTION

WARNINGS SECTION

FOR EXTERNAL USE ONLY Avoid contact with eyes. In case of contact, flush with water. Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, contact a physician.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact the Poison Control Center immediately.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antibacterial Foam

Hand Sanitizer & Protectant

Protects Significantly Longer than Alcohol

Water-Based

Alcohol Free

Entire label includes principal display panelEntire label includes principal display panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN1
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD1
1020365benzalkonium chloride 0.13 % Topical FoamSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130855354005009GTIN-13: 0855354005009
EAN-13: 0855354005009
GTIN-12: 855354005009
UPC-A: 855354005009
GTIN storage (14 digits): 00855354005009		growdefender-antibacterialfoam-1.72oz-label copy.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87109-0013-1GrowDefender Antibacterial Foam50.68 mL in 1 BOTTLE, PUMPSOLUTION50.681

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87109-001387109-0013-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
GrowDefender Antibacterial FoamANTIBACTERIAL FOAMGrow Defender LLC423af3d9-6413-c097-e063-6294a90ae1a92025-10-28WarningsExact identifier
ndc (package): 87109-0013-1
ndc (product): 87109-0013
ndc11 (package): 87109001301
spl id: 423af3d9-6414-c097-e063-6294a90ae1a9
spl set id: 423af3d9-6413-c097-e063-6294a90ae1a9

Reported adverse events (FAERS/openFDA)#

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