KeriCure Fabric and Hand Sanitizer

Manufacturer
Kericure Inc.
Effective date
2020-07-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:21:28

Label at a glance#

ProductKeriCure Fabric and Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Storage and handling

Other Information  • Do not store bottle above 105°F • M ay discolor some fabrics • harmful to some wood finishes

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% (v/v)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Uses • to decrease bacteria on fabrics, clothes, hands, skin & surfaces that could cause disease • for repeated use

Warnings

WARNINGS SECTION

For external use only • Flammable, Keep away from heat or flame • Do not use on children less than 2 months 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 • do NOT ingest • If swallowed, seek medical help or contact a Poison Control Center right away

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

Directions • Shake bottle before use • Spray onto desired area to fully cover the area • Rub into skin where applied or rub hands together • No need to rub into the fabric or surface • Do not over saturate clothing or fabrics • Spot test fabrics prior to use • Adult supervision recommended 

STORAGE AND HANDLING SECTION

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients • Water, glycerin, hydrogen peroxide

SPL UNCLASSIFIED SECTION

Made in the USA 

KILLS MORE THAN 99.9% OF GERMS

UNSCENTED

PREVENT TRANSFER OF GERMS TO CLOTHES, FABRICS, HANDS & SURFACES

KeriCureMedical.com

® KeriCure Inc • All rights reserved

Distributed by KeriCure Inc

3701A Southwestern Blvd. Baltimore MD 21229

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1014638isopropyl alcohol 70 % Topical SprayPSN2
1014638isopropyl alcohol 0.7 ML/ML Topical SpraySCD2
1014638isopropyl alcohol 70 % Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78280-306-042025-01-30C16284748780-12cef2736-a6ef-d83d-e063-dadaa90ab31fKeriCure MEDICAL FABRIC AND HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78280-306-04KeriCure Fabric and Hand Sanitizer115 mL in 1 BOTTLE, SPRAYSPRAY1152

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78280-306KERICURE FABRIC AND HAND SANITIZER (ISOPROPYL ALCOHOL) SPRAY [KERICURE INC.]2Legacy NDC, 1 package rows20200715_f85d5192-0faf-4310-b30a-4cb5b11b034f.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
78280-30678280-306-04

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

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
c7d1f79b-ec71-4b74-9d8d-fb05243e4045f85d5192-0faf-4310-b30a-4cb5b11b034f2020-07-03WarningsExact identifier
spl id: c7d1f79b-ec71-4b74-9d8d-fb05243e4045
spl set id: f85d5192-0faf-4310-b30a-4cb5b11b034f

Reported adverse events (FAERS/openFDA)#

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