warnings
Palabras de advertencia Atención
Gel Antiseptico Dermowipe
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Gel Antiseptico Dermowipe
- Generic name
- GEL ANTISEPTICO A BASE DE ALCOHOL ETILICO
- Manufacturer
- Key Qumica S.A. de C.V.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 15620afc-d6ae-0f34-e063-6294a90a8ad2
- SPL ID
- 2b26aa61-8365-58d9-e063-6294a90ae76b
- Version
- 2
- Effective date
- 2025-01-07
- Source export date
- 2026-10-27
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:57:10
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | 505G(a)(3) | openfda.application_number | |
| brand name | Gel Antiseptico Dermowipe | openfda.brand_name | |
| generic name | GEL ANTISEPTICO A BASE DE ALCOHOL ETILICO | openfda.generic_name | |
| manufacturer name | Key Qumica S.A. de C.V. | openfda.manufacturer_name | |
| ndc | package | 58345-103-05 | openfda.package_ndc |
| ndc | package | 58345-103-04 | openfda.package_ndc |
| ndc | package | 58345-103-08 | openfda.package_ndc |
| ndc | package | 58345-103-01 | openfda.package_ndc |
| ndc | package | 58345-103-06 | openfda.package_ndc |
| ndc | package | 58345-103-02 | openfda.package_ndc |
| ndc | package | 58345-103-07 | openfda.package_ndc |
| ndc | package | 58345-103-03 | openfda.package_ndc |
| ndc | product | 58345-103 | openfda.product_ndc |
| ndc11 | package | 58345010303 | derived:openfda.package_ndc |
| ndc11 | package | 58345010305 | derived:openfda.package_ndc |
| ndc11 | package | 58345010304 | derived:openfda.package_ndc |
| ndc11 | package | 58345010301 | derived:openfda.package_ndc |
| ndc11 | package | 58345010308 | derived:openfda.package_ndc |
| ndc11 | package | 58345010302 | derived:openfda.package_ndc |
| ndc11 | package | 58345010306 | derived:openfda.package_ndc |
| ndc11 | package | 58345010307 | derived:openfda.package_ndc |
| spl id | 2b26aa61-8365-58d9-e063-6294a90ae76b | id | |
| spl set id | 15620afc-d6ae-0f34-e063-6294a90a8ad2 | set_id | |
| unii | 3K9958V90M | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings
Indicaciones de peligro H226 - Líquido y vapores inflamables. H302 - Nocivo en caso de ingestión. H320 - Provoca irritación ocular. H335 - Puede irritar las vías respiratorias. Display Contenido de activos Descripción
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.