Hand Guard

Manufacturer: Anderson Chemical Company
Effective date: 2020-06-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:17:20

Label at a glance#

ProductHand Guard

Active ingredientALCOHOL

Label structure13 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Contacts and useful links#

PhoneLabel contact320-693-2477

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol, 65% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacterial that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age.
on open skin wounds.

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth
in case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash occurs. These may be signs of a serious condition.

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

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, hydrogen peroxide, purified water USP

Other information

OTHER SAFETY INFORMATION

Store between 15-30°C (59-86°F)

Avoid freezing and excessive heat above 40°C (104°F)

Questions or comments?

OTC - QUESTIONS SECTION

320-693-2477

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3785 ml NDC: 63131-9049 Hand Guard Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63131-9049-1	2022-01-28	C162847	48780-1	d6a99b39-40bd-a426-e053-dadaa90af4c2	a7aa8f34-494d-3759-e053-2a95a90acac7
63131-9049-4	2022-01-28	C162847	48780-1	d6a99b39-40bd-a426-e053-dadaa90af4c2	a7aa8f34-494d-3759-e053-2a95a90acac7
63131-9049-5	2022-01-28	C162847	48780-1	d6a99b39-40bd-a426-e053-dadaa90af4c2	a7aa8f34-494d-3759-e053-2a95a90acac7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
63131-9049-1	Hand Guard	3785 mL in 1 JUG	LIQUID	3785	1
63131-9049-1	Hand Guard	7570 in 1 CASE	LIQUID	7570	1
63131-9049-4	Hand Guard	15140 in 1 CASE	LIQUID	15140	1
63131-9049-4	Hand Guard	3785 mL in 1 JUG	LIQUID	3785	1
63131-9049-5	Hand Guard	208175 mL in 1 DRUM	LIQUID	208175	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63131-9049	HAND GUARD (ETHYL ALCOHOL) LIQUID [ANDERSON CHEMICAL COMPANY]	1	Legacy NDC, 5 package rows	20200612_a7aa8f34-494d-3759-e053-2a95a90acac7.zip

Products#

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

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

Hand Guard
Ethyl Alcohol
GLYCERIN
ALCOHOL
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63131-9049	63131-9049-1, 63131-9049-4, 63131-9049-5

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
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	ACTIB
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
a7aa6343-b761-7c2e-e053-2995a90adf57			a7aa8f34-494d-3759-e053-2a95a90acac7	2020-06-09	Warnings	Exact identifier spl id: a7aa6343-b761-7c2e-e053-2995a90adf57 spl set id: a7aa8f34-494d-3759-e053-2a95a90acac7

Reported adverse events (FAERS/openFDA)#

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