Instant hand Sanitizer

Manufacturer
International Fragrances Inc
Effective date
2020-04-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:23

Label at a glance#

ProductInstant hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

hand sanitizer to decrease bacteria on the skin recommended for repeated use for use when soap and water are not available

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping. supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (100F)

Label contents#

Full prescribing information#

Active ingredient:

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 75% v/v

PURPOSE:

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to decrease bacteria on the skin
  • recommended for repeated use
  • for use when soap and water are not available

WARNING:

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame. Do not use in children less than 6 years of age. On open skin wounds.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and allow to dry without wiping.
  • supervise children under 6 years of age when using this product to avoid swallowing

OTHER INFORMATION:

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)

Avoid freezing and excessive heat above 40C (100F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Vitamin E, Aloe Vera

SPL UNCLASSIFIED SECTION

With Vitamin E

Kills 99% of Germs

Product compliant with CARB Regulations. Made in USA

Distributed by IFS, International Fragrance Shop Baltimore, MD.

www.intlfragshop.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

untitleduntitled

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1598066isopropyl alcohol 75 % Topical SprayPSN1
1598066isopropyl alcohol 0.75 ML/ML Topical SpraySCD1
1598066isopropyl alcohol 75 % Topical SpraySY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74462-143-022022-01-28C16284748780-1d6a99b39-3a53-a426-e053-dadaa90af4c2Instant hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74462-143-02Instant hand Sanitizer59.14 mL in 1 BOTTLE, SPRAYSPRAY59.141

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74462-143INSTANT HAND SANITIZER (ISOPROPYL ALCOHOL) SPRAY [INTERNATIONAL FRAGRANCES INC]1Legacy NDC, 1 package rows20200416_2300770a-2449-4104-8093-2ca3bdea792c.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
74462-14374462-143-02

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
904fb010-90a1-468b-979f-256c9b823e3c2300770a-2449-4104-8093-2ca3bdea792c2020-04-15WarningsExact identifier
spl id: 904fb010-90a1-468b-979f-256c9b823e3c
spl set id: 2300770a-2449-4104-8093-2ca3bdea792c

Reported adverse events (FAERS/openFDA)#

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