dicolor Hand Sanitizer Gel

Manufacturer
SODI PINTURAS, S.A. DE C.V.
Effective date
2020-11-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:32:57

Label at a glance#

Productdicolor
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

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

Dosage and administration

Directions Place enough product on hands to cover all surfaces. Rub hands together until dry.

Label contents#

Full prescribing information#

DIRECTIONS DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Inactive ingredients Water (Aqua), Glycerin, Carbomer, Triethanolamine

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Use[s]

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

KEEP OUT OF REACH OF CHILDREN

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.

PURPOSE

OTC - PURPOSE SECTION

Purpose Antmicrobial

WARNINGS AND PRECAUTIONS

WARNINGS AND PRECAUTIONS SECTION

Store below 110°F (43°C)

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

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

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

WARNINGS

WARNINGS SECTION

Warnings

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

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Ethyl Alcohol 70% v/v

ASK A DOCTOR

OTC - ASK DOCTOR/PHARMACIST SECTION

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

STOP USE

OTC - STOP USE SECTION

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

PACKAGE LABELS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DI COLOR HAND SANITIZER GELDI COLOR HAND SANITIZER GEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79050-0040-62022-01-28C16284748780-1d6a99b39-7e31-a426-e053-dadaa90af4c2dicolor Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79050-0040-6dicolor1000 mL in 1 BOTTLEGEL10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79050-0040DICOLOR (ALCOHOL) GEL [SODI PINTURAS, S.A. DE C.V.]2Legacy NDC, 1 package rows20201105_a7dc78e4-583c-9a9e-e053-2995a90a40c7.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
79050-004079050-0040-6

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
b3425f94-30a6-dc2b-e053-2995a90a7106a7dc78e4-583c-9a9e-e053-2995a90a40c72020-11-04WarningsExact identifier
spl id: b3425f94-30a6-dc2b-e053-2995a90a7106
spl set id: a7dc78e4-583c-9a9e-e053-2995a90a40c7

Reported adverse events (FAERS/openFDA)#

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