ALOBON Hand Sanitizer

Manufacturer
Shantou Wanbang Cosmetic Co., Ltd
Effective date
2020-07-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:20

Label at a glance#

ProductALOBON Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 75%v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

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

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

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age
  • on open skin wounds

When using this product;

OTC - WHEN USING SECTION

When using this product; keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact 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 age 6 when using this product avoid swallowing.

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl propanol, chloroxylenol, glycerin, methyl gluceth-10, parfum, water.

Package Label/Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 78692-134-34; 500 ml

Alobon Hand SanitizerAlobon Hand Sanitizer

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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78692-134-342022-01-28C16284748780-1d6a99b39-4249-a426-e053-dadaa90af4c2a821f647-be63-274c-e053-2a95a90a23ce

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78692-134-34ALOBON Hand Sanitizer500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78692-134ALOBON HAND SANITIZER (HAND SANITIZER) GEL [SHANTOU WANBANG COSMETIC CO., LTD]1Legacy NDC, 1 package rows20200715_a821f647-be63-274c-e053-2a95a90a23ce.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78692-13478692-134-34

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
a821f647-be64-274c-e053-2a95a90a23cea821f647-be63-274c-e053-2a95a90a23ce2020-07-09WarningsExact identifier
spl id: a821f647-be64-274c-e053-2a95a90a23ce
spl set id: a821f647-be63-274c-e053-2a95a90a23ce

Reported adverse events (FAERS/openFDA)#

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