FDA.reportPublic FDA data

GLOBAL CHOICE HAND SANITIZER

Manufacturer
RNA PHARMA, LLC
Effective date
2020-04-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:33:03

Label at a glance#

ProductGLOBAL CHOICE HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTACTIVE INGREDIENTACTIVE INGREDIENTACTIVE INGREDIENTACTIVE INGREDIENTACTIVE INGREDIENTACTIVE INGREDIENTACTIVE INGREDIENTACTIVE INGREDIENTACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTSINACTIVE INGREDIENTSINACTIVE INGREDIENTSINACTIVE INGREDIENTSINACTIVE INGREDIENTSINACTIVE INGREDIENTSINACTIVE INGREDIENTSINACTIVE INGREDIENTSINACTIVE INGREDIENTSINACTIVE INGREDIENTS

DOSAGE & ADMINISTRATION SECTION

DOSAGE & ADMINISTRATIONDOSAGE & ADMINISTRATIONDOSAGE & ADMINISTRATIONDOSAGE & ADMINISTRATIONDOSAGE & ADMINISTRATIONDOSAGE & ADMINISTRATIONDOSAGE & ADMINISTRATIONDOSAGE & ADMINISTRATIONDOSAGE & ADMINISTRATIONDOSAGE & ADMINISTRATION

WARNINGS SECTION

WARNINGSWARNINGSWARNINGSWARNINGSWARNINGSWARNINGSWARNINGSWARNINGSWARNINGSWARNINGS

INDICATIONS & USAGE SECTION

INDICATIONS & USAGEINDICATIONS & USAGEINDICATIONS & USAGEINDICATIONS & USAGEINDICATIONS & USAGEINDICATIONS & USAGEINDICATIONS & USAGEINDICATIONS & USAGEINDICATIONS & USAGEINDICATIONS & USAGE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDRENKEEP OUT OF REACH OF CHILDRENKEEP OUT OF REACH OF CHILDRENKEEP OUT OF REACH OF CHILDRENKEEP OUT OF REACH OF CHILDRENKEEP OUT OF REACH OF CHILDRENKEEP OUT OF REACH OF CHILDRENKEEP OUT OF REACH OF CHILDRENKEEP OUT OF REACH OF CHILDRENKEEP OUT OF REACH OF CHILDREN

OTC - PURPOSE SECTION

PURPOSEPURPOSEPURPOSEPURPOSEPURPOSEPURPOSEPURPOSEPURPOSEPURPOSEPURPOSE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE PRINCIPALPACKAGE PRINCIPALPACKAGE PRINCIPALPACKAGE PRINCIPALPACKAGE PRINCIPALPACKAGE PRINCIPALPACKAGE PRINCIPALPACKAGE PRINCIPALPACKAGE PRINCIPALPACKAGE PRINCIPAL

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60717-80560717-805-04, 60717-805-08, 60717-805-02, 60717-805-16, 60717-805-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)132584PQMOIACT
WATER059QF0KO0RIACT
CAPRYLYL GLYCOL00YIU5438UIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302IACT
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
d3c426ab-1a64-3494-e053-2a95a90a9677a47133df-de87-05f6-e053-2a95a90a1fb92021-12-22WarningsExact identifier
spl set id: a47133df-de87-05f6-e053-2a95a90a1fb9

Reported adverse events (FAERS/openFDA)#

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