Hand Sanitizer

Manufacturer
Guangzhou Keman Technology Co., Ltd.
Effective date
2020-05-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:11:00

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Store below 110°F (43°C).

INACTIVE INGREDIENT SECTION

Water,Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Ammonium Hydroxide

INDICATIONS & USAGE SECTION

Put enough product in your palm to cover hands and rub hands together briskly until dry.

OTC - ACTIVE INGREDIENT SECTION

Ethanol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization

WARNINGS SECTION

Flammable. Keep away from fire or flame. For extermal use only When using this product, do not use in or near the eyes. In case of contact, rinse eyes throughly with water. Stop use and ask a doctor if iritation or rash appears and lasts Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN1
1047755ethanol 0.75 ML/ML Topical SolutionSCD1
1047755ethanol 75 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55866-002-012022-01-28C16284748780-1d6a99b39-f261-a426-e053-dadaa90af4c2a56e2223-2696-3cb6-e053-2995a90a4fa6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55866-002-01Hand Sanitizer100 mL in 1 BOTTLELIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55866-002HAND SANITIZER LIQUID [GUANGZHOU KEMAN TECHNOLOGY CO., LTD.]1Legacy NDC, 1 package rows20200513_a56e2223-2696-3cb6-e053-2995a90a4fa6.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
55866-00255866-002-01

Ingredients#

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

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

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
a56e2cb1-275c-4999-e053-2995a90a66c6a56e2223-2696-3cb6-e053-2995a90a4fa62020-05-12WarningsExact identifier
spl id: a56e2cb1-275c-4999-e053-2995a90a66c6
spl set id: a56e2223-2696-3cb6-e053-2995a90a4fa6

Reported adverse events (FAERS/openFDA)#

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