warnings
Warnings
No Drip Severe Anefrin Nasal
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
- No Drip Severe Anefrin Nasal
- Generic name
- 0.05% OXYMETAZOLINE HCL
- Manufacturer
- Walgreens Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c126e969-56f3-47b4-a011-02ff150eccb8
- SPL ID
- 3091b846-549f-496e-8878-404309f6baeb
- Version
- 4
- Effective date
- 2024-08-02
- Source export date
- 2026-11-06
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 08:08:42
| 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 | No Drip Severe Anefrin Nasal | openfda.brand_name | |
| generic name | 0.05% OXYMETAZOLINE HCL | openfda.generic_name | |
| manufacturer name | Walgreens Company | openfda.manufacturer_name | |
| ndc | package | 0363-2350-52 | openfda.package_ndc |
| ndc | product | 0363-2350 | openfda.product_ndc |
| ndc11 | package | 00363235052 | derived:openfda.package_ndc |
| rxcui | 1000990 | openfda.rxcui | |
| spl id | 3091b846-549f-496e-8878-404309f6baeb | id | |
| spl set id | c126e969-56f3-47b4-a011-02ff150eccb8 | set_id | |
| unii | K89MJ0S5VY | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings and cautions
Drug Fact
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.