warnings
Warnings
signature care nasal decongestant
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
- signature care nasal decongestant
- Generic name
- OXYMETAZOLINE HYDROCHLORIDE
- Manufacturer
- Safeway
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f9ac80d1-3753-412b-a407-18a6b50e5d1c
- SPL ID
- 0492955a-6e24-4b31-bf42-3b877a750d3c
- Version
- 3
- Effective date
- 2024-08-27
- Source export date
- 2026-10-12
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:31:09
| Harmonized routes |
|---|
| NASAL |
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 | signature care nasal decongestant | openfda.brand_name | |
| generic name | OXYMETAZOLINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Safeway | openfda.manufacturer_name | |
| ndc | package | 21130-813-10 | openfda.package_ndc |
| ndc | product | 21130-813 | openfda.product_ndc |
| ndc11 | package | 21130081310 | derived:openfda.package_ndc |
| rxcui | 1000990 | openfda.rxcui | |
| spl id | 0492955a-6e24-4b31-bf42-3b877a750d3c | id | |
| spl set id | f9ac80d1-3753-412b-a407-18a6b50e5d1c | set_id | |
| unii | K89MJ0S5VY | 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.