Instant Hand Sanitizer

Manufacturer
American Screening LLC
Effective date
2021-12-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:46:02

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Storage and handling

Store under 105°F

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For rinse-free hand sanitizing to remove 99.9% bacteria on skin.

Warnings

WARNINGS SECTION

​Flammable. Keep away from fire or flame. For external use only.​

When using this product

OTC - WHEN USING SECTION

Do not use in eyes. In case of contact with eyes, rinse with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop and persist.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical health promptly

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

Other Information

STORAGE AND HANDLING SECTION

Store under 105°F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadenisis Leaf, Glycerin, Hydroxypropylcellulose, Vitamin E, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4 ounces (118 mL) - NDC 00000-000-00

label-4ozlabel-4oz

8 ounces (236 mL) - NDC 00000-000-00

label-8ozlabel-8oz

16 ounces (437 mL) - NDC 00000-000-00

label-16ozlabel-16oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN4
582753ethanol 0.7 ML/ML Topical SolutionSCD4
582753ethanol 70 % Topical SolutionSY4
582753ethyl alcohol 70 % Topical SolutionSY4

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73817-100-04Instant Hand Sanitizer0.118 L in 1 BOTTLE, SPRAYSOLUTION0.1184
73817-100-08Instant Hand Sanitizer0.236 L in 1 BOTTLE, SPRAYSOLUTION0.2364
73817-100-16Instant Hand Sanitizer0.473 L in 1 BOTTLE, SPRAYSOLUTION0.4734

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73817-100INSTANT HAND SANITIZER (HAND SANITIZER) SOLUTION [AMERICAN SCREENING LLC]4Legacy NDC, 3 package rows20211230_3ce56a5e-6ced-4ec4-ab84-bcba2e7ceebc.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73817-10073817-100-04, 73817-100-08, 73817-100-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
f77392f2-f02c-4ded-84b6-ca20eb7f19e63ce56a5e-6ced-4ec4-ab84-bcba2e7ceebc2021-12-29WarningsExact identifier
spl id: f77392f2-f02c-4ded-84b6-ca20eb7f19e6
spl set id: 3ce56a5e-6ced-4ec4-ab84-bcba2e7ceebc

Reported adverse events (FAERS/openFDA)#

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