FDA.reportPublic FDA data

Antibacterial Hand Sanitizer

Manufacturer
Twintech Industry, Inc.
Effective date
2022-01-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:18:03

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

• pump as needed into your palms and thoroughly spread on both hands • rub into skin until dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • decreases bacteria and germs on the hands
  • when water, soap & towel are not available
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only
Flammable. Keep away from fire or flame

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops or persists.

Do not apply around eyes.

OTC - DO NOT USE SECTION

Do not use

OTC - DO NOT USE SECTION

in ears & mouth

When using this product,

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact flush eyes with water.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children under 6, use only under adult supervision. Not recommended for infants.

Directions

DOSAGE & ADMINISTRATION SECTION

  • pump as needed into your palms and thoroughly spread on both hands
  • rub into skin until dry

Other information

OTHER SAFETY INFORMATION

  • store at 20 ℃ (68 ℃ to 77 ℉).
  • may discolor fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified water, triethanolamine, glycerine, Disodium EDTA, carbomer

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antibacterial Hand Sanitizer
1.8 fl. oz. (54ML)


Distributed by:
TWINTECH INDUSTRY, INC.
Cerritos, CA          Made in China

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Label

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
76700-30976700-309-01, 76700-309-02, 76700-309-03, 76700-309-04, 76700-309-05

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
EDETATE DISODIUM7FLD91C86KIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT

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
13ea2ef3-c836-443e-b146-8066b0b090da1f53e99f-b3c2-4b02-a534-c7346d8be09d2022-07-20WarningsExact identifier
spl set id: 1f53e99f-b3c2-4b02-a534-c7346d8be09d

Reported adverse events (FAERS/openFDA)#

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