FDA.reportPublic FDA data

ALBY SPRAY SANITIZER 60ML

Manufacturer
K-Zoe Marketing
Effective date
2020-11-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:35:01

Label at a glance#

ProductALBY SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

For areas and surfaces to decrease bacteria and germs.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride .13%.

Purpuse

OTC - PURPOSE SECTION

Antiseptic.

Uses

INSTRUCTIONS FOR USE SECTION

For areas and surfaces to decrease bacteria and germs.

Warnings

WARNINGS AND PRECAUTIONS SECTION

For external use only. Keep away from heat or flame.

WARNINGS SECTION

Avoid contact with eyes

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep away from children

WARNINGS SECTION

If swallowed get medical attention right away.

Instructions

DOSAGE & ADMINISTRATION SECTION

Apply directly over surface, let it dry.

Other Info

OTHER SAFETY INFORMATION

Store between 15° - 30°C (59°F - 86°F). Avoid freezing and excessive heat above 40°C (104°F).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, fragance.

Don´t Use

OTC - DO NOT USE SECTION

Don´t use in children less than 2 months of age. On open skin wounds.

INDICATIONS & USAGE SECTION

Spray Sanitizer

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039012benzalkonium chloride 0.13 % Topical SprayPSN1
1039012benzalkonium chloride 1.3 MG/ML Topical SpraySCD1
1039012benzalkonium chloride 0.13 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80686-001-602022-01-28C16284748780-1d6a99b3a-003f-a426-e053-dadaa90af4c2ALBY SPRAY SANITIZER 60ML

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80686-001-60ALBYSANITIZER60 mL in 1 BOTTLE, SPRAYSPRAY601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80686-001ALBY SANITIZER (ANTICEPTIC BENZALCONIUM CHLORIDE SPRAY) SPRAY [K-ZOE MARKETING]1Legacy NDC, 1 package rows20201211_b4e62c6f-3a3f-0792-e053-2995a90a7119.zip

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
80686-00180686-001-60

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
GLYCERINPDC6A3C0OXIACT
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
b4e62c6f-3a40-0792-e053-2995a90a7119b4e62c6f-3a3f-0792-e053-2995a90a71192020-11-25WarningsExact identifier
spl id: b4e62c6f-3a40-0792-e053-2995a90a7119
spl set id: b4e62c6f-3a3f-0792-e053-2995a90a7119

Reported adverse events (FAERS/openFDA)#

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