FDA.reportPublic FDA data

Hand Sanitizer Spray

Manufacturer
Beacon Promotions, Inc. | Beacon Promotions Inc.
Effective date
2024-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:49:33

Label at a glance#

ProductSANSPRAY-NA
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Spray enough product on hands to cover all surfaces. Rub hands together until dry.

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings:

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame. Keep out of eyes, ears
& mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask doctor if
redness or irritation develop and persist for more than 72 hours. Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Do not use on children less than 2 months of age. Do not use on open skin wounds.

Directions

INSTRUCTIONS FOR USE SECTION

Spray enough product on hands to cover
all surfaces. Rub hands together until dry.

Inactive Ingredient:

INACTIVE INGREDIENT SECTION

Water, Aloe Vera, Glycerin, Propylene Glycol, Tocopherol, Lemon Fragrance.

Purpose

INDICATIONS & USAGE SECTION

Anticeptic

Drug Facts

DOSAGE & ADMINISTRATION SECTION

Active Ingredient Purpose
Benzalkonium Chloride (0.1%)

Spray enough product on hands to cover
all surfaces. Rub hands together until dry.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SSNASSNA

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1052947benzalkonium chloride 0.1 % Topical SprayPSN2
1052947benzalkonium chloride 1 MG/ML Topical SpraySCD2
1052947benzalkonium chloride 0.1 % Topical SpraySY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70445-606-01SANSPRAY-NA9.76 mL in 1 BOTTLE, SPRAYSPRAY9.762

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70445-606SANSPRAY-NA (NON-ALCOHOL ANTIBACTERIAL HAND SANITIZER) SPRAY [BEACON PROMOTIONS, INC.]21 package rows20250101_0e0fef1d-85bf-e65e-e063-6294a90ab631.zip

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
70445-60670445-606-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOEV5VD430YW9IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT

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
2a932c8f-3a4b-dfcd-e063-6394a90ac20b0e0fef1d-85bf-e65e-e063-6294a90ab6312024-12-31WarningsExact identifier
spl id: 2a932c8f-3a4b-dfcd-e063-6394a90ac20b
spl set id: 0e0fef1d-85bf-e65e-e063-6294a90ab631

Reported adverse events (FAERS/openFDA)#

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