warnings
Warnings
McKesson Phenylephrine HCl
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
- McKesson Phenylephrine HCl
- Generic name
- PHENYLEPHRINE HCL
- Manufacturer
- McKesson Medical-Surgical
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e09060f7-ca0b-5f7c-e053-2995a90ab344
- SPL ID
- 266bbe87-c019-f406-e063-6394a90a516c
- Version
- 3
- Effective date
- 2024-11-08
- 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 02:52:39
| Harmonized routes |
|---|
| ORAL |
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 | M012 | openfda.application_number | |
| brand name | McKesson Phenylephrine HCl | openfda.brand_name | |
| generic name | PHENYLEPHRINE HCL | openfda.generic_name | |
| manufacturer name | McKesson Medical-Surgical | openfda.manufacturer_name | |
| ndc | package | 68599-1631-3 | openfda.package_ndc |
| ndc | product | 68599-1631 | openfda.product_ndc |
| ndc11 | package | 68599163103 | derived:openfda.package_ndc |
| rxcui | 1299145 | openfda.rxcui | |
| spl id | 266bbe87-c019-f406-e063-6394a90a516c | id | |
| spl set id | e09060f7-ca0b-5f7c-e053-2995a90ab344 | set_id | |
| unii | 04JA59TNSJ | 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.