FDA.reportPublic FDA data

Scented Hand Sanitizer

Manufacturer
Beacon Promotions, Inc.
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:32:26

Label at a glance#

ProductScented Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

■ Put enough product in your palm to cover your hands and rub together briskly until dry ■ Children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

Drug Facts

DOSAGE & ADMINISTRATION SECTION

Ethyl alcohol 63.5

Put enough product in your palm to cover your hands and rub together
briskly until dry

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria on the skin

Warnings

WARNINGS SECTION


Flammable. Keep away from fire or flame.

■ For external use only.

■ When using this product do notuse in or near the eyes. In case of contact, rinse eyes thoroughly with water.

■ Stop use andask a doctor if irritation or rash appears and lasts.

■ Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Directions

INSTRUCTIONS FOR USE SECTION

■ Put enough product in your palm to cover your hands and rub together
briskly until dry

■ Children under 6 years of age should be supervised when using this
product

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 63.5 w/w

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/ VP Copolymer Hydroxypropyl Methylcellulose, Mannitol, Microcrystalline Cellulose, Parfum, Propylene Glycol, Aqua, Tocopheryl Acetate

Other

OTHER SAFETY INFORMATION

■ Store at room temperature

■ May discolor certain fabrics or surfaces

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LEMLEM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2003712ethanol 63.5 % Topical GelPSN2
2003712ethanol 0.635 ML/ML Topical GelSCD2
2003712ethanol 63.5 % Topical GelSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70445-608-01Scented Hand Sanitizer15 mL in 1 BOTTLEGEL152
70445-608-02Scented Hand Sanitizer30 mL in 1 BOTTLEGEL302
70445-608-03Scented Hand Sanitizer60 mL in 1 BOTTLEGEL602
70445-608-04Scented Hand Sanitizer120 mL in 1 BOTTLEGEL1202
70445-608-05Scented Hand Sanitizer240 mL in 1 BOTTLEGEL2402
70445-608-06Scented Hand Sanitizer240 mL in 1 BOTTLE, PUMPGEL2402
70445-608-07Scented Hand Sanitizer300 mL in 1 BOTTLE, PUMPGEL3002
70445-608-08Scented Hand Sanitizer480 mL in 1 BOTTLEGEL4802
70445-608-09Scented Hand Sanitizer480 mL in 1 BOTTLE, PUMPGEL4802

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
70445-60870445-608-01, 70445-608-02, 70445-608-03, 70445-608-04, 70445-608-05, 70445-608-06, 70445-608-07, 70445-608-08, 70445-608-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT

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
Scented Hand SanitizerSCENTED HAND SANITIZERBeacon Promotions, Inc.1f95444c-7587-a07e-e063-6394a90af5342026-01-12WarningsExact identifier
ndc (package): 70445-608-04
ndc (package): 70445-608-03
ndc (package): 70445-608-08
ndc (package): 70445-608-05
ndc (package): 70445-608-01
ndc (package): 70445-608-07
ndc (package): 70445-608-02
ndc (package): 70445-608-09
ndc (package): 70445-608-06
ndc (product): 70445-608
ndc11 (package): 70445060807
ndc11 (package): 70445060805
ndc11 (package): 70445060803
ndc11 (package): 70445060802
ndc11 (package): 70445060804
ndc11 (package): 70445060808
ndc11 (package): 70445060809
ndc11 (package): 70445060801
ndc11 (package): 70445060806
spl id: 48390f5d-ba29-7c28-e063-6294a90a2d7e
spl set id: 1f95444c-7587-a07e-e063-6394a90af534

Reported adverse events (FAERS/openFDA)#

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