FDA.reportPublic FDA data

A2A HAND SANITIZER

Manufacturer
RNA PHARMA, LLC
Effective date
2020-06-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:23:53

Label at a glance#

ProductA2A HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

active ingredientsactive ingredientsactive ingredientsactive ingredientsactive ingredientsactive ingredientsactive ingredientsactive ingredientsactive ingredientsactive ingredientsactive ingredientsactive ingredients

INACTIVE INGREDIENT SECTION

inactive ingredientsinactive ingredientsinactive ingredientsinactive ingredientsinactive ingredientsinactive ingredientsinactive ingredientsinactive ingredientsinactive ingredientsinactive ingredientsinactive ingredientsinactive ingredients

DOSAGE & ADMINISTRATION SECTION

dosage & administrationdosage & administrationdosage & administrationdosage & administrationdosage & administrationdosage & administrationdosage & administrationdosage & administrationdosage & administrationdosage & administrationdosage & administrationdosage & administration

WARNINGS SECTION

warningswarningswarningswarningswarningswarningswarningswarningswarningswarningswarningswarnings

INDICATIONS & USAGE SECTION

indications & usageindications & usageindications & 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 childrenkeep out of reach of childrenkeep out of reach of children

OTC - PURPOSE SECTION

purposepurposepurposepurposepurposepurposepurposepurposepurposepurposepurposepurpose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label principalpackage label principalpackage label principalpackage label principalpackage label principalpackage label principalpackage label principalpackage label principalpackage label principalpackage label principalpackage label principalpackage label 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
60717-80460717-804-04, 60717-804-02, 60717-804-08, 60717-804-16, 60717-804-32, 60717-804-01

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
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)132584PQMOIACT
CAPRYLYL GLYCOL00YIU5438UIACT
ISOPROPYL ALCOHOLND2M416302IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT

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
d3c3a312-bec7-1c56-e053-2995a90a8362a5b664e8-7e22-10c5-e053-2995a90a94492021-12-22WarningsExact identifier
spl set id: a5b664e8-7e22-10c5-e053-2995a90a9449

Reported adverse events (FAERS/openFDA)#

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