Severe Nasal Congestion
- Product NDC
- 0363-9351
- 11-digit product format
- 003639351
- Labeler code
- 0363
- Product ID
- 0363-9351_5bc7c9ed-0b5c-3775-e063-6394a90a2642
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxymetazoline Spray
- Dosage form
- LIQUID
- Route
- NASAL
- Labeler
- Walgreens Company
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-07-10
- Substance
- OXYMETAZOLINE HYDROCHLORIDE
- Active strength
- 50 mg/100mL
- Pharmacologic classes
- Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Severe Nasal Congestion
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| OXYMETAZOLINE HYDROCHLORIDE | 50 mg/100mL |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|
| 0363-9351-75 | 00363935175 | 1 BOTTLE, PUMP in 1 CARTON (0363-9351-75) / 22 mL in 1 BOTTLE, PUMP | 2026-07-10 | No | No | Current |