FDA.reportPublic FDA data

KeriCure Hand Sanitizer

Manufacturer
Kericure Inc.
Effective date
2025-01-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:54:14

Label at a glance#

ProductKeriCure Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other Information - Do not store product above 105°F May discolor some fabrics • harmful to wood finishes

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% (v/v)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Uses • to decrease bacteria on the skin that could cause disease • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only • Flammable, keep away from heat or flame • Do not use in children less than 2 month of age • on open skin wounds • When using this product keep out of eyes, ears and mouth • In case of contact with eyes, rinse eyes thoroughly with water

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children • If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

Directions • Shake bottle before use • Spray enough product on hands to cover all surfaces • Rub hands together until dry • Adult supervision

STORAGE AND HANDLING SECTION

Other Information- Do not store product above 105°F May discolor some fabrics • harmful to wood finishes

INACTIVE INGREDIENT SECTION

Inactive Ingredients- Water, isopropyl alcohol, aloe barbadensis, glycerine, mentha piperita (pepper-mint) (fragrance), cellulose, tocophoryl acetate

SPL UNCLASSIFIED SECTION

■ SCENTED    ■ UNSCENTED

MEDICAL

Made in the USA

KILLS MORE THAN 99.9% OF GERMS

FORMULATED FOR PROFESSIONALS

GENTLE ENOUGH FOR EVERYDAY USE

WITH ALOE & VITAMIN E

SKIN MOISTURIZERS

KeriCureMedical.com

® KeriCure Inc • All rights reserved

Distributed by KeriCure Inc 3701A Southwestern Blvd. Baltimore MD 21229

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KeriCure® HAND SANITIZERKeriCure® HAND SANITIZER

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN3
1041849ethanol 0.7 ML/ML Topical SpraySCD3
1041849ethanol 70 % Topical SpraySY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78280-302-012025-02-01C16284748780-12cef2736-7e00-d83d-e063-dadaa90ab31fKeriCure ® HAND SANITIZER
78280-302-022025-02-01C16284748780-12cef2736-7e00-d83d-e063-dadaa90ab31fKeriCure ® HAND SANITIZER
78280-302-042025-02-01C16284748780-12cef2736-7e00-d83d-e063-dadaa90ab31fKeriCure ® HAND SANITIZER
78280-302-082025-02-01C16284748780-12cef2736-7e00-d83d-e063-dadaa90ab31fKeriCure ® HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78280-302-01KeriCure Hand Sanitizer28 mL in 1 BOTTLE, SPRAYSPRAY283
78280-302-02KeriCure Hand Sanitizer55 mL in 1 BOTTLE, SPRAYSPRAY553
78280-302-04KeriCure Hand Sanitizer115 mL in 1 BOTTLE, SPRAYSPRAY1153
78280-302-08KeriCure Hand Sanitizer230 mL in 1 BOTTLE, SPRAYSPRAY2303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78280-302KERICURE HAND SANITIZER (ALCOHOL) SPRAY [KERICURE INC.]3Current NDC, Legacy NDC, 4 package rows20250202_de516d2e-9c16-4bd2-b4c2-7e2f9fd26442.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78280-30278280-302-01, 78280-302-02, 78280-302-04, 78280-302-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16IACT
MENTHA X PIPERITA WHOLE79M2M2UDA9IACT

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
KeriCure Hand SanitizerALCOHOLKericure Inc.de516d2e-9c16-4bd2-b4c2-7e2f9fd264422025-01-22WarningsExact identifier
ndc (package): 78280-302-01
ndc (package): 78280-302-02
ndc (package): 78280-302-04
ndc (package): 78280-302-08
ndc (product): 78280-302
ndc11 (package): 78280030204
ndc11 (package): 78280030208
ndc11 (package): 78280030202
ndc11 (package): 78280030201
spl id: 6d220d4b-a2a9-488c-b38f-360a4e3b57ff
spl set id: de516d2e-9c16-4bd2-b4c2-7e2f9fd26442

Reported adverse events (FAERS/openFDA)#

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