COLLOID 5050 G

Manufacturer
COLLOIDS DE MEXICO, S.A. DE C.V.
Effective date
2020-08-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:23:46

Label at a glance#

ProductCOLLOID 5050 G
Active ingredientALCOHOL
Label structure12 sections

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excesive heat above 40C (104F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol 73% v/v. Purpose: Antiseptic.

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • In 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.

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation accurs. 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.

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.

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)

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

INACTIVE INGREDIENT SECTION

Purified water USP, Carbomer L, Triethanolamine, Diethanolamine, Monoethanolamine, Monopropylene Glycol.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

etiqueta c5050getiqueta c5050getiqueta atras C5050Getiqueta atras C5050G

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286987ethanol 73 % Topical GelPSN2
2286987ethanol 0.73 ML/ML Topical GelSCD2
2286987ethanol 73 % Topical GelSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
424daadb-95de-8ece-97f5-235e3f7f0001Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79306-011-152022-01-28C16284748780-1d6a99b39-4497-a426-e053-dadaa90af4c2aaf9259e-ae3c-696d-e053-2a95a90a6a9b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79306-011-15COLLOID 5050 G836 g in 1 BOTTLE, DISPENSINGGEL8362

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79306-011COLLOID 5050 G (ALCOHOL HAND SANITIZER) GEL [COLLOIDS DE MEXICO, S.A. DE C.V.]2Legacy NDC, 1 package rows20200805_aaf9259e-ae3c-696d-e053-2a95a90a6a9b.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79306-01179306-011-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
ac12a2f6-b42a-2397-e053-2a95a90a98f9aaf9259e-ae3c-696d-e053-2a95a90a6a9b2020-08-04WarningsExact identifier
spl id: ac12a2f6-b42a-2397-e053-2a95a90a98f9
spl set id: aaf9259e-ae3c-696d-e053-2a95a90a6a9b

Reported adverse events (FAERS/openFDA)#

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