Major Nasal Decongestant
- Product NDC
- 68071-3858
- 11-digit product format
- 680713858
- Labeler code
- 68071
- Product ID
- 68071-3858_36b1eb59-ef20-3e53-e063-6294a90ab5ab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxymetazoline hydrochloride
- Dosage form
- SPRAY
- Route
- NASAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-12-31
- Substance
- OXYMETAZOLINE HYDROCHLORIDE
- Active strength
- .5 mg/mL
- Pharmacologic classes
- Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| K89MJ0S5VY | OXYMETAZOLINE HYDROCHLORIDE | 2315-02-8 | OXYMETAZOLINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3858-3 | 68071385803 | 1 BOTTLE, PUMP in 1 CARTON (68071-3858-3) / 30 mL in 1 BOTTLE, PUMP | 2023-12-31 | No | No | Historical |