HAND AND SKIN DISINFECTANT SPRAY

Manufacturer
MOLECULE KORUYUCU SAGLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI
Effective date
2020-07-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:20:04

Label at a glance#

ProductHand and Skin Sanitizer
Active ingredientALCOHOL, BENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Apply to the entire surface of your hands. It is recommended to be used in its original packaging as per hygiene rules

Storage and handling

Store between 15-30 ºC Avoid freezing and excessive heat above 40 ºC

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

70% Alcohol Denat, 0.1% Benzalkonium Chloride

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

A ready-to-use product. Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to the entire surface of your hands. It is recommended to be used in its original packaging as per hygiene rules

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

■ on children less than 2 months of age

■ on open skin wounds

OTC - WHEN USING SECTION

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes throughly with water. keep warm and rest the patient.

If breathing is irregular or stops, give artificial respiration. If unconscious, place in a healing position and seek medical attention immediately. Do not give anything by mouth.
If swallowed: DO NOT vomit. Rinse your mouth with water. Never give anything by mouth to an unconscious patient. Get medical attention immediately.
In case of skin contact: Avoid prolonged contact. Get medical attention if symptoms persist. Remove contaminated clothing and shoes and isolate them. Frozen clothes on the skin must be thawed before removing them. In contact with the liquefied gas, thaw the iced pieces with warm water.
In case of contact with eyes: Rinse eyelids for at least 15 minutes with plenty of water and seek medical attention.

OTC - STOP USE SECTION

If irritation and redness develops and persists.

In case of poisoning, call the National Emergency Services immediately.

Symptoms of poisoning: Dizziness, loss of consciousness, speech impairment.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, contact a doctor or Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Melaleuca Alternifolia Leaf Extract, Hypericum Perforatum Extract, Glycyrrhiza Glabra Root Extract, Aqua

Other Informations

STORAGE AND HANDLING SECTION

Store between 15-30 ºC
Avoid freezing and excessive heat above 40 ºC

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

Products#

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DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79781-20679781-206-01, 79781-206-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
e8ce18e1-3852-a3fe-e053-2995a90a0241a9d852de-ab99-81fa-e053-2995a90a4e702022-09-16WarningsExact identifier
spl set id: a9d852de-ab99-81fa-e053-2995a90a4e70

Reported adverse events (FAERS/openFDA)#

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