ALCOHOL HAND SANITIZER

Manufacturer
GUANGDONG THEAOSON TECHNOLOGY CO.,LTD
Effective date
2020-12-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:35:26

Label at a glance#

ProductALCOHOL HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

Keep away from the source of fire and flame. For external use only.

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age
on open skin wounds, damaged, inflamed or broken skin.

OTC - WHEN USING SECTION

When using this product, keep out of eyes, ears, and mouth. Use only under adult supervision. In case of contact with eyes, rinse eyes thoroughly with water.
Non staining, may discolor certain fabrics. People who are allergic to alchohol shuld use this product with caution.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

78792-012-01 50ML

78792-012-01 50ML78792-012-01 50ML

78792-012-02 100ML

78792-012-02 100ML78792-012-02 100ML

78792-012-03 182ML

78792-012-03 182ML78792-012-03 182ML

78792-012-04 478ML

78792-012-04 478ML78792-012-04 478ML

78792-012-05 494ML

78792-012-05 494ML78792-012-05 494ML

78792-012-06 1000ML

78792-012-06 1000ML78792-012-06 1000ML

78792-012-07 5000ML

78792-012-07 5000ML78792-012-07 5000ML

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78792-012-01ALCOHOL HAND SANITIZER50 mL in 1 BOTTLEGEL501
78792-012-02ALCOHOL HAND SANITIZER100 mL in 1 BOTTLEGEL1001
78792-012-03ALCOHOL HAND SANITIZER182 mL in 1 BOTTLEGEL1821
78792-012-04ALCOHOL HAND SANITIZER478 mL in 1 BOTTLEGEL4781
78792-012-05ALCOHOL HAND SANITIZER494 mL in 1 BOTTLEGEL4941
78792-012-06ALCOHOL HAND SANITIZER1000 mL in 1 BOTTLEGEL10001
78792-012-07ALCOHOL HAND SANITIZER5000 mL in 1 BOTTLEGEL50001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78792-012ALCOHOL HAND SANITIZER GEL [GUANGDONG THEAOSON TECHNOLOGY CO.,LTD]1Legacy NDC, 7 package rows20201217_b68cbf9f-37c4-d6aa-e053-2a95a90a4197.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78792-01278792-012-01, 78792-012-05, 78792-012-04, 78792-012-03, 78792-012-06, 78792-012-02, 78792-012-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
b68ca27d-b801-4aac-e053-2a95a90aa3f9b68cbf9f-37c4-d6aa-e053-2a95a90a41972020-12-15WarningsExact identifier
spl id: b68ca27d-b801-4aac-e053-2a95a90aa3f9
spl set id: b68cbf9f-37c4-d6aa-e053-2a95a90a4197

Reported adverse events (FAERS/openFDA)#

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