FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Phoenix Wipes Inc
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:47

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient70 % Alcohol vv Purpose: Antiseptic

DOSAGE & ADMINISTRATION SECTION

DosageDosage

INACTIVE INGREDIENT SECTION

InactiveInactive

INDICATIONS & USAGE SECTION

Indication and UsageIndication and Usage

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of ChildrenKeep out of Children

OTC - PURPOSE SECTION

Propose SectionPropose Section

WARNINGS SECTION

Warning SectionWarning Section

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package Picturepackage Picture2ml NDC 78837-202-20

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78837-202-202022-01-28C16284748780-1d6a99b39-4040-a426-e053-dadaa90af4c2a79f29b7-02ea-1156-e053-2995a90a7a83

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78837-202-20Hand Sanitizer1 mL in 1 PACKETGEL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78837-202HAND SANITIZER (ALCOHOL, WATER) GEL [PHOENIX WIPES INC]1Legacy NDC, 1 package rows20200616_a79f29b7-02ea-1156-e053-2995a90a7a83.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78837-20278837-202-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
1-(3,4-DIMETHOXYPHENYL)PROPANE-1,2-DIOLN6222F124LIACT

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
a79f29b7-02eb-1156-e053-2995a90a7a83a79f29b7-02ea-1156-e053-2995a90a7a832020-06-08WarningsExact identifier
spl id: a79f29b7-02eb-1156-e053-2995a90a7a83
spl set id: a79f29b7-02ea-1156-e053-2995a90a7a83

Reported adverse events (FAERS/openFDA)#

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