FDA.reportPublic FDA data

Antibacterial Hand Sanitizer

Manufacturer
Webb Business Promotions, Inc | Webb Business Promotions,Inc
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 23:46:20

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Squeeze enough product on hands to cover all surfaces. Rub hands together untill dry.

Storage and handling

Store at 20 C (68-77 F). May discolore fabrics

Label contents#

Full prescribing information#

Warnings

WARNINGS SECTION

For external use only. Flammable

OTC - DO NOT USE SECTION

Do not use on children less than 2 month of age. Do not use on open skin wounds.

OTC - ASK DOCTOR SECTION

Stop use and ask doctor if redeness or irritation develop and persist for more than 72 hours

OTC - STOP USE SECTION

Stop use and ask doctor if redenss or irritation develop and persist for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

STORAGE AND HANDLING SECTION

Store at 20 C (68-77 F). May discolore fabrics

Purpose

OTC - PURPOSE SECTION

Antiseptic

Directions

DOSAGE & ADMINISTRATION SECTION

Squeeze enough product on hands to cover all surfaces. Rub hands together untill dry.

OTHER SAFETY INFORMATION

Keep away from heat and flame. Keep out of eyes, ears, and mouth.

INDICATIONS & USAGE SECTION

Squezze enough product on hands to cover all surfaces. Rub hands together untill dry.

Active Ingridient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Inactive Ingridient section

INACTIVE INGREDIENT SECTION

Trolamine. Water. Propylene Glycol. Aloe Vera. Carbomer. Glycerine.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antibacterial Hand Sanitizer GelAntibacterial Hand Sanitizer Gel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN6
581660ethanol 0.62 ML/ML Topical GelSCD6
581660ethanol 62 % Topical GelSY6

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70445-416-022023-07-28C16284748780-10191ceaa-719d-198a-e063-dbdaa90aec3eAntibacterial Hand Sanitizer
70445-416-082023-07-28C16284748780-10191ceaa-719d-198a-e063-dbdaa90aec3eAntibacterial Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70445-416-02Antibacterial Hand Sanitizer60 mL in 1 BOTTLEGEL606
70445-416-08Antibacterial Hand Sanitizer240 mL in 1 BOTTLEGEL2406

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70445-416ANTIBACTERIAL HAND SANITIZER (ALCOHOL) GEL [WEBB BUSINESS PROMOTIONS, INC]6Legacy NDC, 2 package rows20220105_b1ccfc52-7431-40d3-e053-2a95a90a20cb.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70445-41670445-416-02, 70445-416-08

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
CARBOMER 9404Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
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
d4c50bf7-3f20-a89b-e053-2a95a90a3602b1ccfc52-7431-40d3-e053-2a95a90a20cb2022-01-04WarningsExact identifier
spl id: d4c50bf7-3f20-a89b-e053-2a95a90a3602
spl set id: b1ccfc52-7431-40d3-e053-2a95a90a20cb

Reported adverse events (FAERS/openFDA)#

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