Antibacterial Hand Sanitizer

Manufacturer
Hubei Flex Daily Chemicals CO., LTD
Effective date
2022-08-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:50:21

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Squirt as needed into your palms and thoroughly spread on both hands, rub into skin until dry.

Storage and handling

Store st 20C (68-77F) May discolor some fabrics

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Fact

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%. 

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacterial on the skkin when water, soap and towel are not available

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame

Do not apply around eyes. Do not use in ears and mouth.

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes.  In case of contact, flush eyes with water

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children must be spervised when use this product.

Directions

DOSAGE & ADMINISTRATION SECTION

Squirt as needed into your palms and thoroughly spread on both hands, rub into skin until dry.

Other information

STORAGE AND HANDLING SECTION

Store st 20C (68-77F)

May discolor some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, triethanolamine, carbomer, Vitamin E, aloe barbadensis leaf extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81131-001-01Antibacterial Hand Sanitizer15 mL in 1 BOTTLEGEL152
81131-001-02Antibacterial Hand Sanitizer30 mL in 1 BOTTLEGEL302
81131-001-03Antibacterial Hand Sanitizer35 mL in 1 BOTTLEGEL352
81131-001-04Antibacterial Hand Sanitizer60 mL in 1 BOTTLEGEL602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81131-001ANTIBACTERIAL HAND SANITIZER (ALCOHOL) GEL [HUBEI FLEX DAILY CHEMICALS CO., LTD]2Legacy NDC, 4 package rows20220811_47349a42-08f4-48cd-acc0-0fd541d447be.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
81131-00181131-001-01, 81131-001-02, 81131-001-03, 81131-001-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
e5eb3c90-55a4-5490-e053-2995a90a1dbc47349a42-08f4-48cd-acc0-0fd541d447be2022-08-10WarningsExact identifier
spl id: e5eb3c90-55a4-5490-e053-2995a90a1dbc
spl set id: 47349a42-08f4-48cd-acc0-0fd541d447be

Reported adverse events (FAERS/openFDA)#

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