FDA.reportPublic FDA data

Unscented 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#

ProductUnscented Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Directions ■ 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

Antimicrobial

Warnings

WARNINGS SECTION

Warnings
Flammable. Keep away from fire or flame.

■ For external use only.

■ When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

■ Stop use and ask 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

Directions

■ 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

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

Other Information

OTHER SAFETY INFORMATION

■ Store at room temperature

■ May discolor certain fabrics or surfaces

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UnsUns

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
70445-609-01Unscented Sanitizer15 mL in 1 BOTTLEGEL152
70445-609-02Unscented Sanitizer30 mL in 1 BOTTLEGEL302
70445-609-03Unscented Sanitizer60 mL in 1 BOTTLEGEL602
70445-609-04Unscented Sanitizer120 mL in 1 BOTTLEGEL1202
70445-609-05Unscented Sanitizer240 mL in 1 BOTTLEGEL2402
70445-609-06Unscented Sanitizer240 mL in 1 BOTTLE, PUMPGEL2402
70445-609-07Unscented Sanitizer300 mL in 1 BOTTLE, PUMPGEL3002
70445-609-08Unscented Sanitizer480 mL in 1 BOTTLEGEL4802
70445-609-09Unscented 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
70445-60970445-609-01, 70445-609-02, 70445-609-03, 70445-609-04, 70445-609-05, 70445-609-07, 70445-609-06, 70445-609-08, 70445-609-09

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
PROPYLENE GLYCOL6DC9Q167V3IACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
Unscented SanitizerUNSCENTED SANITIZERBeacon Promotions, Inc.1f96aecf-8ca2-aa27-e063-6394a90abb792026-01-12WarningsExact identifier
ndc (package): 70445-609-06
ndc (package): 70445-609-09
ndc (package): 70445-609-03
ndc (package): 70445-609-07
ndc (package): 70445-609-01
ndc (package): 70445-609-08
ndc (package): 70445-609-02
ndc (package): 70445-609-04
ndc (package): 70445-609-05
ndc (product): 70445-609
ndc11 (package): 70445060906
ndc11 (package): 70445060907
ndc11 (package): 70445060904
ndc11 (package): 70445060902
ndc11 (package): 70445060901
ndc11 (package): 70445060903
ndc11 (package): 70445060905
ndc11 (package): 70445060909
ndc11 (package): 70445060908
spl id: 48390f5d-ba28-7c28-e063-6294a90a2d7e
spl set id: 1f96aecf-8ca2-aa27-e063-6394a90abb79

Reported adverse events (FAERS/openFDA)#

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