FDA.reportPublic FDA data

Handy Doctor Hand Sanitizer

Manufacturer
Sauber Co.,Ltd.
Effective date
2021-01-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:58

Label at a glance#

ProductHandy Doctor Hand Sanitizer
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BlisterBlister [Blister]

StickerSticker [Sticker]

OTC - ACTIVE INGREDIENT SECTION

OTC - ASK DOCTOR SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

INACTIVE INGREDIENT SECTION

WARNINGS SECTION

OTHER SAFETY INFORMATION

DOSAGE & ADMINISTRATION SECTION

INDICATIONS & USAGE SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020364ethanol 62 % Topical SprayPSN1
1020364ethanol 0.62 ML/ML Topical SpraySCD1
1020364ethanol 62 % Topical SpraySY1
1020364ethyl alcohol 62 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78880-017-022023-01-30C16284748780-1f386c649-ebf1-0266-e053-dadaa90a7c1aHandy Doctor Hand Sanitizer 78880-017-02

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78880-017-02Handy Doctor Hand Sanitizer1 in 1 BLISTER PACKSPRAY11
78880-017-02Handy Doctor Hand Sanitizer17 mL in 1 CASESPRAY171

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78880-017HANDY DOCTOR HAND SANITIZER (ALCOHOL) SPRAY [SAUBER CO.,LTD.]1Legacy NDC, 2 package rows20210115_b8e8faa1-b121-450e-e053-2995a90aeace.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
78880-01778880-017-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
CALENDULA OFFICINALIS WHOLEPFR03EBU0HIACT
WATER059QF0KO0RIACT

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
b8e8faa1-b122-450e-e053-2995a90aeaceb8e8faa1-b121-450e-e053-2995a90aeace2021-01-14Exact identifier
spl id: b8e8faa1-b122-450e-e053-2995a90aeace
spl set id: b8e8faa1-b121-450e-e053-2995a90aeace

Reported adverse events (FAERS/openFDA)#

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