Qwix Hand Sanitizer

Manufacturer
SORA KOZMETIK SANAYI TICARET ANONIM SIRKETI
Effective date
2020-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:24

Label at a glance#

ProductQwix Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

to help reduce bacteria on the skin that may cause disease.

Dosage and administration

Spray hands thoroughly with product and rub into hands until dry.

Storage and handling

Store at room temperature or in a cool place.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 90.24%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to help reduce bacteria on the skin that may cause disease.

Warnings

WARNINGS SECTION

For external use only.
DANGER: Flammable. Contents Under Pressure.
Do not use near heat, sparks, or flames. Vapors may ignite explosively & cause flash fire. Prevent build-up of vapors. Do not smoke. Turn off pilot light, stoves, heaters, and other sources of ignition during use and until all vapors are gone. Do not puncture or incinerate container. Do not expose to heat or store at temperatures about 120F. Use with adequate ventilation.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops.

OTC - WHEN USING SECTION

Avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical attention.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets: Children under 6 years age should be supervised by an adult when using. If swallowed, get medical help or contact your Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray hands thoroughly with product and rub into hands until dry.

Other Information

STORAGE AND HANDLING SECTION

Store at room temperature or in a cool place.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Panthenol (Vitamin B5), Glycerol, Tocopheryl Acetate (Vitamin E), Aloe Barbadensis (Aloe Vera) Leaf Juice.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2375039ethanol 90.2 % Topical SprayPSN1
2375039ethanol 0.902 ML/ML Topical SpraySCD1
2375039ethanol 90.2 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77462-005-052022-01-28C16284748780-1d6a99b39-f7c2-a426-e053-dadaa90af4c2Qwix Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77462-005-05Qwix Hand Sanitizer150 mL in 1 BOTTLE, SPRAYAEROSOL1501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77462-005QWIX HAND SANITIZER (ETHYL ALCOHOL) AEROSOL [SORA KOZMETIK SANAYI TICARET ANONIM SIRKETI]1Legacy NDC, 1 package rows20200715_aa6ad3de-a5f0-575c-e053-2a95a90a1336.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77462-00577462-005-05

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
aa6ad3de-a5f1-575c-e053-2a95a90a1336aa6ad3de-a5f0-575c-e053-2a95a90a13362020-07-14WarningsExact identifier
spl id: aa6ad3de-a5f1-575c-e053-2a95a90a1336
spl set id: aa6ad3de-a5f0-575c-e053-2a95a90a1336

Reported adverse events (FAERS/openFDA)#

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