Dr. Disin Hand Sanitizer

Manufacturer
CNF Trading Group
Effective date
2020-10-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:32:07

Label at a glance#

ProductDr. Disin Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient [s]

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

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

Warnings:

WARNINGS SECTION

For external use only. Flammable, keep away from heat or flame.

Do not use:

OTC - DO NOT USE SECTION

In children less than 2 months of age. On open skin wounds.

When using this product:

OTC - WHEN USING SECTION

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop Use and ask a doctor:

OTC - STOP USE SECTION

If irritation or rash occur, These may be signs of a serious condition.

Keep out of reach of children:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 children under 6 years of age when using this product to avoid swallowing.

Other Information:

SPL UNCLASSIFIED SECTION

Store between 15-30°C (59-86°F).

Avoid freezing and excessive heat above 40°C (104°F).

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Glycerol, Carbomer, Triethanolamine, Water.

Package Labeling:79205-000-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:79205-000-10

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79205-000-022021-07-23C16284748780-1c7ccaba7-1c98-fd44-e053-dadaa90aa01bDr. Disin Hand Sanitizer
79205-000-102021-07-23C16284748780-1c7ccaba7-1c98-fd44-e053-dadaa90aa01bDr. Disin Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79205-000-02Dr. Disin Hand Sanitizer60 mL in 1 BOTTLEGEL602
79205-000-10Dr. Disin Hand Sanitizer300 mL in 1 BOTTLEGEL3002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79205-000DR. DISIN HAND SANITIZER (ALCOHOL) GEL [CNF TRADING GROUP]2Legacy NDC, 2 package rows20201021_ad54f616-0aa7-2c06-e053-2a95a90a742e.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79205-00079205-000-02, 79205-000-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
b21f30d1-22cf-3703-e053-2a95a90ac6abad54f616-0aa7-2c06-e053-2a95a90a742e2020-10-20WarningsExact identifier
spl id: b21f30d1-22cf-3703-e053-2a95a90ac6ab
spl set id: ad54f616-0aa7-2c06-e053-2a95a90a742e

Reported adverse events (FAERS/openFDA)#

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