Lifebuoy Hand Sanitizer

Manufacturer
Guangdong Essence Daily Chemical Co., Ltd
Effective date
2020-05-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:02

Label at a glance#

ProductLifebuoy 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 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 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

  • Onchildren less than 2 months of age
  • On open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact, rinse eyes thoroughly with water.

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

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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water USP, Acrylates Copolymer, Glycerin, Triethanolamine, Aminomethyl Propanol

SPL UNCLASSIFIED SECTION

other information

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

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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
73931-006-012025-01-30C16284748780-12cef2736-77e7-d83d-e063-dadaa90ab31f19203434-0c11-46cd-b529-a9dc6b25fb51
73931-006-022025-01-30C16284748780-12cef2736-77e7-d83d-e063-dadaa90ab31f19203434-0c11-46cd-b529-a9dc6b25fb51

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73931-006-01Lifebuoy Hand Sanitizer50 mL in 1 BOTTLEGEL501
73931-006-02Lifebuoy Hand Sanitizer500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73931-006LIFEBUOY HAND SANITIZER (ALCOHOL) GEL [GUANGDONG ESSENCE DAILY CHEMICAL CO., LTD]1Legacy NDC, 2 package rows20200508_19203434-0c11-46cd-b529-a9dc6b25fb51.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73931-00673931-006-01, 73931-006-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML · Source PDF

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
7b0005b3-feed-46bf-8af5-5508c3813b2719203434-0c11-46cd-b529-a9dc6b25fb512020-05-07WarningsExact identifier
spl id: 7b0005b3-feed-46bf-8af5-5508c3813b27
spl set id: 19203434-0c11-46cd-b529-a9dc6b25fb51

Reported adverse events (FAERS/openFDA)#

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