Antibacterial Hand Sanitizer

Manufacturer: Sweda Company LLC
Effective date: 2022-01-03
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 22:19:21

Label at a glance#

ProductAntibacterial Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

Hand sanitizer to help decrease bacteria on the skin. When water, soap & towel are not available. Recommended for repeated use.

Dosage and administration

Squirt as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 72%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria on the skin. When water, soap & towel are not available. Recommended for repeated use.

Warnings:

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame. Do not apply around eyes,

Do not use

OTC - DO NOT USE SECTION

in ears & mouth.

When using this product,

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Directions:

DOSAGE & ADMINISTRATION SECTION

Squirt as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Other Information:

SPL UNCLASSIFIED SECTION

Store at 20° C (68° to 77° F). May discolor fabrics

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

water

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 · 3 matching rows.

Antibacterial Hand Sanitizer
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
90121-004	90121-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	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
d4b08741-d934-9423-e053-2a95a90a010b			bb79329d-d5b5-631f-e053-2a95a90af781	2022-01-03	Warnings	Exact identifier spl id: d4b08741-d934-9423-e053-2a95a90a010b spl set id: bb79329d-d5b5-631f-e053-2a95a90af781

Reported adverse events (FAERS/openFDA)#

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