Redusa Hand Sanitizer

Manufacturer: REDUSA GLOBAL KOZMETIK KISISEL BAKIM URUNLERI SANAYI VE TICARET LIMITED SIRKETI
Effective date: 2020-07-07
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:20:28

Label at a glance#

ProductRedusa Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

to help reduce bacteria on the skin. For use when soap and water are not available.

Dosage and administration

*Put enough product in your palm to cover hands and rub hands together until dry. *Children under 6 years should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to help reduce bacteria on the skin. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

*Flammable

*Keep away from source of heat of fire

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse throughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental Ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

*Put enough product in your palm to cover hands and rub hands together until dry.

*Children under 6 years should be supervised when using this product.

Other Information

SPL UNCLASSIFIED SECTION

*Store at a temperature below 110 °F (43° C).

*May discolor certain fabrics or surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Isopropyl Alcohol, Glycerin, Isopropyl Aminomethyl Propanol, Fragrance (Parfum).

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79275-000-08	2022-01-28	C162847	48780-1	d6a99b39-c47a-a426-e053-dadaa90af4c2	Redusa Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79275-000-08	Redusa Hand Sanitizer	250 mL in 1 BOTTLE	GEL	250		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79275-000	REDUSA HAND SANITIZER (ALCOHOL) GEL [REDUSA GLOBAL KOZMETIK KISISEL BAKIM URUNLERI SANAYI VE TICARET LIMITED SIRKETI]	1	Legacy NDC, 1 package rows	20200708_a9df19f9-8b03-5caf-e053-2a95a90aa22d.zip

Products#

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

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

Redusa Hand Sanitizer
ALCOHOL
WATER
ISOPROPYL ALCOHOL
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79275-000	79275-000-08

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
ISOPROPYL ALCOHOL	ND2M416302	IACT
GLYCERIN	PDC6A3C0OX	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
a9df0f20-180a-8db0-e053-2a95a90aaa66			a9df19f9-8b03-5caf-e053-2a95a90aa22d	2020-07-07	Warnings	Exact identifier spl id: a9df0f20-180a-8db0-e053-2a95a90aaa66 spl set id: a9df19f9-8b03-5caf-e053-2a95a90aa22d

Reported adverse events (FAERS/openFDA)#

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