Hyaluronic Acid

Manufacturer
Quimfa S.A
Effective date
2020-06-05
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:32:55

Label at a glance#

ProductHyaluronic Acid
Active ingredientHYALURONIC ACID
Label structure2 sections

Label contents#

Full prescribing information#

Precautions and Warnings

PRECAUTIONS SECTION

* Si se observase derrame articular extraerlo antes de inyectar Maxiostenil.
* Es necesario seguir la técnica correcta de la inyección intraarticular en condiciones completamente asépticas.
Ver Instrucciones de uso y manipulación.
* Como en cualquier procedimiento intraarticular, es recomendable evitar la sobrecarga de la articulación
tratada, inmediatamente después de la inyección intraarticular.
* Los pacientes deben ser cuidadosamente examinados antes de la administración de Maxiostenil para
determinar posibles signos de inflamación agudos y el médico debe evaluar cuidadosamente la oportunidad del
inicio de la terapia.
* Se debe observar particular atención en pacientes con infecciones o alteraciones de la piel en zonas próximas
al punto de inyección para evitar la posibilidad de desarrollar artritis bacteriana.

* Guardar fuera del alcance de los niños.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

hyaluronic acidhyaluronic acid

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77651-4162-62022-01-28C16284748780-1d6a99b39-c2a3-a426-e053-dadaa90af4c2a75e2bb2-f89a-53f4-e053-2a95a90a93c7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77651-4162-6Hyaluronic Acid1 in 1 SYRINGEINJECTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77651-4162HYALURONIC ACID INJECTION [QUIMFA S.A]1Legacy NDC, 1 package rows20200616_a75e2bb2-f89a-53f4-e053-2a95a90a93c7.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77651-416277651-4162-6

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
HYALURONIC ACIDS270N0TRQYACTIB

Source Document#

Source XML

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog.

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
a75e2bb2-f89b-53f4-e053-2a95a90a93c7a75e2bb2-f89a-53f4-e053-2a95a90a93c72020-06-05Exact identifier
spl id: a75e2bb2-f89b-53f4-e053-2a95a90a93c7
spl set id: a75e2bb2-f89a-53f4-e053-2a95a90a93c7

Reported adverse events (FAERS/openFDA)#

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