FDA.reportPublic FDA data

Advanced Hand Sanitizer

Manufacturer
Hive9 Protection, LLC
Effective date
2021-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:45:45

Label at a glance#

ProductAdvanced Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Hive9 Protection’s Advanced Hand Sanitizer provides revolutionary protection in an alcohol-free formula. The scientifically-proven solution kills harmful germs, bacteria, and microbes, and gently soothes and softens skin with aloe vera. Recommended for repeated use. 

Dosage and administration

Apply liberally to the palms of the hands or areas of damaged skin. Rub into skin until dry. Recommended for repeated use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

PURPOSE:

OTC - PURPOSE SECTION

Hand & Skin Sanitizer

USES:

INDICATIONS & USAGE SECTION

Hive9 Protection’s Advanced Hand Sanitizer provides revolutionary protection in an alcohol-free formula. The scientifically-proven solution kills harmful germs, bacteria, and microbes, and gently soothes and softens skin with aloe vera. Recommended for repeated use. 

WARNINGS:

WARNINGS SECTION

  • Do not freeze 
  • For external use only 

Do not use

OTC - DO NOT USE SECTION

  • in ears, eyes or mouth

When using this product,

OTC - WHEN USING SECTION

  • avoid contact with the eyes 
  • In case of contact, flush eyes with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • redness or irritation develops and persists for more than 72 hours

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

Apply liberally to the palms of the hands or areas of damaged skin. Rub into skin until dry. Recommended for repeated use.

OTHER INFORMATION:

SPL UNCLASSIFIED SECTION

Store in a cool dry place below 104° F (40°C)

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, Laureth-4, Polyhexanide, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

Package Labeling: 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81739-00181739-001-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
CAPRYLYL GLUCOSIDEV109WUT6RLIACT
LAURETH-46HQ855798JIACT
POLIHEXANIDE322U039GMFIACT
PHENOXYETHANOLHIE492ZZ3TIACT
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDEXGN40YQC7BIACT
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
f27820d9-cb1b-4d89-e053-2995a90a0852c108e9db-0631-d43d-e053-2995a90a5a952023-01-17WarningsExact identifier
spl set id: c108e9db-0631-d43d-e053-2995a90a5a95

Reported adverse events (FAERS/openFDA)#

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