warnings
Warnings
12 Hour Original 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
- 12 Hour Original Nasal Decongestant
- Generic name
- NASAL SPRAY
- Manufacturer
- WinCo Foods LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b3b6065a-56da-45e9-b89d-f6553bc181c9
- SPL ID
- 36a14e66-29e9-4055-8c8b-dc76136021ce
- Version
- 3
- Effective date
- 2024-11-21
- Source export date
- 2026-10-12
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:25:46
| 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 | 12 Hour Original Nasal Decongestant | openfda.brand_name | |
| generic name | NASAL SPRAY | openfda.generic_name | |
| manufacturer name | WinCo Foods LLC | openfda.manufacturer_name | |
| ndc | package | 67091-378-08 | openfda.package_ndc |
| ndc | product | 67091-378 | openfda.product_ndc |
| ndc11 | package | 67091037808 | derived:openfda.package_ndc |
| rxcui | 1000990 | openfda.rxcui | |
| spl id | 36a14e66-29e9-4055-8c8b-dc76136021ce | id | |
| spl set id | b3b6065a-56da-45e9-b89d-f6553bc181c9 | 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.