FDA.reportPublic FDA data

Instant hand sanitizer

Manufacturer
THE BIGBOND LLC
Effective date
2021-02-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:37:43

Label at a glance#

ProductInstant hand sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

1.5m1-3 5ml/time; Store below 110°F (43°C) ; May discolor certain fabrics of surfaces

WARNINGS SECTION

keep out of reach of childen

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Glycerin, Propylene Glycol ,Isopropyl Myristate, Tocopheryl Acetate, Carbomer, Aminomethyl Propanol

INDICATIONS & USAGE SECTION

Take appropriate amount of this product to moisten your hands and rub for one minute until the liquid covers the whole surface

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out oreeceh of cildlen

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

003 8 oz color003 8 oz color

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
87052-017-012023-01-30C16284748780-1f386c64a-0592-0266-e053-dadaa90a7c1aa19ae763-76bd-de1f-e053-2a95a90a5b4a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87052-017-01Instant hand sanitizer236 mL in 1 BOTTLE, PLASTICLIQUID2362

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
87052-017INSTANT HAND SANITIZER (HAND SANITIZER) LIQUID [THE BIGBOND LLC]2Legacy NDC, 1 package rows20210204_a19ae763-76bd-de1f-e053-2a95a90a5b4a.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87052-01787052-017-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ISOPROPYL ALCOHOLND2M416302IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALOE VERA LEAFZY81Z83H0XIACT
CAPRYLYL GLYCOL00YIU5438UIACT
GLYCERINPDC6A3C0OXIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
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
ba6b01ef-bf38-da1a-e053-2a95a90a5b78a19ae763-76bd-de1f-e053-2a95a90a5b4a2021-02-03WarningsExact identifier
spl id: ba6b01ef-bf38-da1a-e053-2a95a90a5b78
spl set id: a19ae763-76bd-de1f-e053-2a95a90a5b4a

Reported adverse events (FAERS/openFDA)#

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