warnings
Avoid contact with skin an eyes. Irritation hazard if spilled or splashed.
CITRACID-50
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
- CITRACID-50
- Generic name
- DESINFECTANT SOLUTION FOR HEMODIALYSIS MACHINE
- Manufacturer
- Aqua Medica, S.A. de C.V.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 040713e7-67cd-8eb0-e063-6394a90aa2a9
- SPL ID
- 43486bf7-f87e-f437-e063-6394a90a338c
- Version
- 3
- Effective date
- 2025-11-10
- Source export date
- 2026-10-12
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:54:23
| Harmonized routes |
|---|
| HEMODIALYSIS |
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 |
|---|---|---|---|
| brand name | CITRACID-50 | openfda.brand_name | |
| generic name | DESINFECTANT SOLUTION FOR HEMODIALYSIS MACHINE | openfda.generic_name | |
| manufacturer name | Aqua Medica, S.A. de C.V. | openfda.manufacturer_name | |
| ndc | package | 81943-701-01 | openfda.package_ndc |
| ndc | product | 81943-701 | openfda.product_ndc |
| ndc11 | package | 81943070101 | derived:openfda.package_ndc |
| spl id | 43486bf7-f87e-f437-e063-6394a90a338c | id | |
| spl set id | 040713e7-67cd-8eb0-e063-6394a90aa2a9 | set_id | |
| unii | 2968PHW8QP | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.