Hand Prep Antiseptic Hand Sanitizer

Manufacturer: Sanco Industries, Inc.
Effective date: 2021-07-19
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 22:40:17

Label at a glance#

ProductHand Prep Antiseptic Hand Sanitizer

Active ingredientISOPROPYL ALCOHOL

Label structure8 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

Contacts and useful links#

PhoneLabel contact1 (260)-426-6281

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 72.2%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only
Flammable, keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

in the eyes
on open skin wounds

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation and redness develop
Condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

Other Information

SPL UNCLASSIFIED SECTION

Store between 59-104°F (15-30°C). Avoid freezing and excessive heat above 104°F (40°C)
May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, glycerin, methacrylic acid ethyl acrylate polymer, FD&C Blue No. 1

Questions or comments

OTC - QUESTIONS SECTION

(260)-426-6281

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Hand Prep Antiseptic Hand Sanitizer
ISOPROPYL ALCOHOL
WATER
GLYCERIN
FD&C BLUE NO. 1

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80248-000	80248-000-01

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
ISOPROPYL ALCOHOL	ND2M416302	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
c77f5c3b-b219-6e26-e053-2a95a90a9c3e			aee4900d-64dc-df72-e053-2a95a90a9013	2021-07-19	Warnings	Exact identifier spl id: c77f5c3b-b219-6e26-e053-2a95a90a9c3e spl set id: aee4900d-64dc-df72-e053-2a95a90a9013

Reported adverse events (FAERS/openFDA)#

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