oxymetazoline hydrochloride
- Product NDC
- 68071-3422
- 11-digit product format
- 680713422
- Labeler code
- 68071
- Product ID
- 68071-3422_36b1caf3-8f0e-088c-e063-6394a90a6a07
- 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
- 2005-12-05
- Marketing end
- 2027-02-28
- Substance
- OXYMETAZOLINE HYDROCHLORIDE
- Active strength
- .05 g/100mL
- Pharmacologic classes
- Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
- NDC exclude flag
- No
- 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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3422-1 | 68071342201 | 1 BOTTLE, SPRAY in 1 CARTON (68071-3422-1) / 30 mL in 1 BOTTLE, SPRAY | 2023-05-31 | 2027-02-28 | No | No | Historical |