HAND-I-SAN

Manufacturer: ZECO, LLC
Effective date: 2025-06-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:03:06

Label at a glance#

ProductHAND-I-SAN

Active ingredientISOPROPYL ALCOHOL

Label structure12 sections

Indications and uses

To help reduce bacteria on the skin that could potenitally cause disease Helps to prevent cross-contamination Recommended for repeated use

Dosage and administration

Wet hands thoroughly, covering entire surface of hands, especially the fingernails and cuticles Rub hands thoroughly until dry

Contacts and useful links#

PhoneLabel contact800-782-0233

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin that could potenitally cause disease
Helps to prevent cross-contamination
Recommended for repeated use

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

Do not use in or near eyes

OTC - STOP USE SECTION

Stop use and consult a doctor if redness or irritation develops.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical attention or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly, covering entire surface of hands, especially the fingernails and cuticles
Rub hands thoroughly until dry

Other information

OTHER SAFETY INFORMATION

Store between 15°C to 30°C (59°F to 86°F)
Avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, hydrogen peroxide

Questions?

OTC - QUESTIONS SECTION

Contact Zee Company at 800-782-0233

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HAND-I-SAN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1039900	isopropyl alcohol 75 % Topical Solution	PSN	1
1039900	isopropyl alcohol 0.75 ML/ML Topical Solution	SCD	1
1039900	isopropyl alcohol 75 % Topical Solution	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829
5eb9f24b-9328-475e-af0a-18021935eb6a	Product name	1	20180220

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
85820-900-01	HAND-I-SAN	3.78 L in 1 JUG	LIQUID	3.78	1
85820-900-02	HAND-I-SAN	18.29 L in 1 PAIL	LIQUID	18.29	1
85820-900-03	HAND-I-SAN	208.17 L in 1 DRUM	LIQUID	208.17	1
85820-900-04	HAND-I-SAN	1040.87 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK	LIQUID	1040.87	1
85820-900-11	HAND-I-SAN	4 in 1 BOX	LIQUID	4	1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

HAND-I-SAN
75% Isopropyl Alcohol Hand Sanitizer
ISOPROPYL ALCOHOL
GLYCERIN
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85820-900	85820-900-01, 85820-900-11, 85820-900-02, 85820-900-03, 85820-900-04

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
ISOPROPYL ALCOHOL	ND2M416302	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
WATER	059QF0KO0R	IACT

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
HAND-I-SAN	75% ISOPROPYL ALCOHOL HAND SANITIZER	ZECO, LLC	37627a51-cf31-013c-e063-6294a90ae13a	2025-06-13	Warnings	Exact identifier ndc (package): 85820-900-04 ndc (package): 85820-900-03 ndc (package): 85820-900-11 ndc (package): 85820-900-02 ndc (package): 85820-900-01 ndc (product): 85820-900 ndc11 (package): 85820090011 ndc11 (package): 85820090004 ndc11 (package): 85820090001 ndc11 (package): 85820090002 ndc11 (package): 85820090003 spl id: 37627a51-cf32-013c-e063-6294a90ae13a spl set id: 37627a51-cf31-013c-e063-6294a90ae13a

Reported adverse events (FAERS/openFDA)#

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