FDA.reportPublic FDA data

glanHealth - Sanitizing Body Spray Advanced

Manufacturer
Dalrada Health Products
Effective date
2020-10-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:12:23

Label at a glance#

ProductglanHealth Sanitizing Body Advanced
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

First aid anti-microbial, topical sanitizer, and antiseptic spray that helps eliminate harmful germs and bacteria on the skin and body. For external use only. For lasting protection, repeated use is recommended.

Dosage and administration

Spray liberally over the body and personal clothing for protection. Recommended for repeated application. Product is safe on all materials and fabrics.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.10%

PURPOSE

OTC - PURPOSE SECTION

Spray sanitizer for the skin and body

USES:

INDICATIONS & USAGE SECTION

First aid anti-microbial, topical sanitizer, and antiseptic spray that helps eliminate harmful germs and bacteria on the skin and body. For external use only. For lasting protection, repeated use is recommended.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Spray liberally over the body and personal clothing for protection. Recommended for repeated application. Product is safe on all materials and fabrics.

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 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

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Aqua, Citric Acid, Laureth-4, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

QUESTIONS?

OTC - QUESTIONS SECTION

1(855) 8692-1526, Mon-Fri 9:00AM-5:00PM (PST)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Pacakge Labeling:59ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

Pacakge Labeling:3.78L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4Bottle4

Pacakge Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label6Label6

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77071-00277071-002-00, 77071-002-01, 77071-002-02, 77071-002-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
LAURETH-46HQ855798JIACT
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
0d9e2768-1f62-e3a1-e063-6394a90a07beb1a0dbf3-eee4-44b8-b008-93219042d7b62023-12-28WarningsExact identifier
spl set id: b1a0dbf3-eee4-44b8-b008-93219042d7b6

Reported adverse events (FAERS/openFDA)#

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