FDA.reportPublic FDA data

not have

Manufacturer
Guangzhou Branson Biotechnology Co., Ltd
Effective date
2020-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:08:40

Label at a glance#

Productnot have
Active ingredientALCOHOL
Label structure6 sections

Storage and handling

Store below 110°F(43°C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%±5(v/v)

Use

INDICATIONS & USAGE SECTION

Decreases bacteria on hands

Warnings

WARNINGS SECTION

Flammable:Keep away from flame or high heat.

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.

Other information

STORAGE AND HANDLING SECTION

Store below 110°F(43°C)

May discolor certain fabrics or surfaces

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 ml label50 ml label60 ml label60 ml label100 ml label100 ml label200 ml label200 ml label250 ml label250 ml label300 ml label300 ml label500 ml label500 ml label

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
75436-001-012021-07-23C16284748780-1c7ccaba7-168f-fd44-e053-dadaa90aa01bAnti Bacterial Hand Sanitizer
75436-001-022021-07-23C16284748780-1c7ccaba7-168f-fd44-e053-dadaa90aa01bAnti Bacterial Hand Sanitizer
75436-001-032021-07-23C16284748780-1c7ccaba7-168f-fd44-e053-dadaa90aa01bAnti Bacterial Hand Sanitizer
75436-001-042021-07-23C16284748780-1c7ccaba7-168f-fd44-e053-dadaa90aa01bAnti Bacterial Hand Sanitizer
75436-001-052021-07-23C16284748780-1c7ccaba7-168f-fd44-e053-dadaa90aa01bAnti Bacterial Hand Sanitizer
75436-001-062021-07-23C16284748780-1c7ccaba7-168f-fd44-e053-dadaa90aa01bAnti Bacterial Hand Sanitizer
75436-001-072021-07-23C16284748780-1c7ccaba7-168f-fd44-e053-dadaa90aa01bAnti Bacterial Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75436-001-01not have50 mL in 1 BOTTLEGEL501
75436-001-02not have60 mL in 1 BOTTLEGEL601
75436-001-03not have100 mL in 1 BOTTLEGEL1001
75436-001-04not have200 mL in 1 BOTTLEGEL2001
75436-001-05not have250 mL in 1 BOTTLEGEL2501
75436-001-06not have300 mL in 1 BOTTLEGEL3001
75436-001-07not have500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75436-001NOT HAVE (ANTI BACTERIAL HAND SANITIZER) GEL [GUANGZHOU BRANSON BIOTECHNOLOGY CO., LTD]1Legacy NDC, 7 package rows20200429_a4671950-f2aa-7036-e053-2a95a90a8dbb.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75436-00175436-001-01, 75436-001-02, 75436-001-03, 75436-001-04, 75436-001-05, 75436-001-06, 75436-001-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
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
a4665dbe-708a-8043-e053-2a95a90a6f92a4671950-f2aa-7036-e053-2a95a90a8dbb2020-04-28WarningsExact identifier
spl id: a4665dbe-708a-8043-e053-2a95a90a6f92
spl set id: a4671950-f2aa-7036-e053-2a95a90a8dbb

Reported adverse events (FAERS/openFDA)#

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