FDA.reportPublic FDA data

Soeder Hand Sanitizer

Manufacturer
Soeder GmbH
Effective date
2020-10-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:10:29

Label at a glance#

ProductSoeder Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

Hand sanitizer to reduce bacteria on skin. For use when soap and water are not available.

Dosage and administration

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

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Ethyl Alcohol 70% v/v...........Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to reduce bacteria on skin. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For External Use Only.

Flammable. Keep away from heat or flame.

OTC - DO NOT USE SECTION

Do not use

  • on children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth.

In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritatin or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. 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 chidlren under 6 years of age when using this product to avoid swallowing.

Other Information

STORAGE AND HANDLING SECTION

store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua/Water, Glycerin, Aloe Barbadensis Extract, Lavandula Angustifolia (Lavender) Oil, Rosmarinus Officinalis (Rosemary) Extract, Salvia Officinalis (Sage) Leaf, Rosmarinus Officinalis Leaf Oil, Citric Acid, Sodium Hydroxide, Linalool, Limonene, Geraniol

Questions or Comments

OTC - QUESTIONS SECTION

Call + 1 212 575-2373 Monday through Friday, 9am-5pm (GMT-4).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80531-00180531-001-01, 80531-001-02, 80531-001-03, 80531-001-04, 80531-001-05, 80531-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
LINALOOL, (+/-)-D81QY6I88EIACT
LIMONENE, (+)-GFD7C86Q1WIACT
ROSEMARYIJ67X351P9IACT
GERANIOLL837108USYIACT
SAGE065C5D077JIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
LAVENDER OILZBP1YXW0H8IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ROSEMARY OIL8LGU7VM393IACT
SODIUM HYDROXIDE55X04QC32IIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0c46601a-573d-956e-e063-6394a90afaf6b21d73ba-ed32-f535-e053-2995a90a11e72023-12-11WarningsExact identifier
spl set id: b21d73ba-ed32-f535-e053-2995a90a11e7

Reported adverse events (FAERS/openFDA)#

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