FDA.reportPublic FDA data

glanHealth Sanitizing Hand Wipe Advanced

Manufacturer
Dalrada Health Products
Effective date
2020-11-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:07:37

Label at a glance#

ProductglanHealth Sanitizing Hand Wipe Advanced
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Cleans and sanitizes the skin and dcreases bacteria. Recommended for single use.

Dosage and administration

WIPE LIBERALLY OVER THE HANDS, RUB INTO SKIN UNTIL DRY. RECOMMENDED FOR SINGLE USE.

Label contents#

Full prescribing information#

DIRECTIONS FOR USE:

DOSAGE & ADMINISTRATION SECTION

WIPE LIBERALLY OVER THE HANDS, RUB INTO SKIN UNTIL DRY. RECOMMENDED FOR SINGLE USE.

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

PURPOSE:

OTC - PURPOSE SECTION

Antiseptic / hand and skin sanitizer

USES:

INDICATIONS & USAGE SECTION

Cleans and sanitizes the skin and dcreases bacteria. Recommended for single use.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

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

WARNINGS:

WARNINGS SECTION

DO NOT FREEZE. FOR EXTERNAL USE ONLY. 

DO NOT USE

OTC - DO NOT USE SECTION

IN EARS, EYES, OR MOUTH.

  • Avoid contact with the eyes. In case of contact, flush eyes with water

Stop use and ask a doctor 

OTC - STOP USE SECTION

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

Keep out of reach fo children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Children should be supervised when using this product.

QUESTIONS?

OTC - QUESTIONS SECTION

1(855) 862-1526, Mon-Fri 9:00AM-5:00PM (CST)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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
77071-00977071-009-00

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
0d9e1544-67c9-ef98-e063-6394a90a0768b3d8d781-9330-82c3-e053-2a95a90a34962023-12-28WarningsExact identifier
spl set id: b3d8d781-9330-82c3-e053-2a95a90a3496

Reported adverse events (FAERS/openFDA)#

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