FDA.reportPublic FDA data

Anti-Bacterial Hand Sanitizer

Manufacturer
GUANGZHOU ZUOFUN COSMETICS CO., LTD.
Effective date
2021-01-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:28

Label at a glance#

ProductAnti-Bacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

FOR HANDWASHING TO DECREASE BACTERIA ON THE HAND

Dosage and administration

WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOUT WIPING.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • FOR HANDWASHING TO DECREASE BACTERIA ON THE HAND

Warnings

WARNINGS SECTION

  • FOR EXTERNAL USE ONLY. FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME
  • DO NOT USE IN THE EYES

STOP USE AND ASK A DOCTOR IF:

  • IRRITATION AND REDNESS DEVELOP
  • CONDITION PERSISTS FOR MORE THAN 72 HOURS

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • IF SWALLOWED, GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER RIGHT AWAY

Directions

DOSAGE & ADMINISTRATION SECTION

WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOUT WIPING.

Other Information

SPL UNCLASSIFIED SECTION

CUSTOMER SUPPORT OR TO REPORT A SERIOUS ADVERSE EVENT, CONTACT 1-888-986-3861

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA, PROPYLENE GLYCOL, GLYCEROL, CARBOMER, AMINOMETHYL PROPANOL

Product Image

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77027-112-012023-07-28C16284748780-10191ceaa-6bcc-198a-e063-dbdaa90aec3eAnti-Bacterial Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77027-112-01Anti-Bacterial Hand Sanitizer60 mL in 1 BOTTLE, PLASTICGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77027-112ANTI-BACTERIAL HAND SANITIZER (ALCOHOL) GEL [GUANGZHOU ZUOFUN COSMETICS CO., LTD.]1Legacy NDC, 1 package rows20210106_baf26dc0-1cc0-4cd8-99df-bf9234f443bf.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77027-11277027-112-01

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
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALCOHOL3K9958V90MACTIB

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
b82dfc94-73dc-1aa6-e053-2995a90a30d5baf26dc0-1cc0-4cd8-99df-bf9234f443bf2021-01-05WarningsExact identifier
spl id: b82dfc94-73dc-1aa6-e053-2995a90a30d5
spl set id: baf26dc0-1cc0-4cd8-99df-bf9234f443bf

Reported adverse events (FAERS/openFDA)#

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