Nasal
- Product NDC
- 0113-2304
- 11-digit product format
- 001132304
- Labeler code
- 0113
- Product ID
- 0113-2304_962b294a-cbef-44f2-a818-7f029dfae86e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- oxymetazoline hydrochloride
- Dosage form
- SPRAY
- Route
- NASAL
- Labeler
- L. Perrigo Company
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 1991-07-29
- Marketing end
- 2022-07-31
- Substance
- OXYMETAZOLINE HYDROCHLORIDE
- Active strength
- 0 g/100mL
- Pharmacologic classes
- Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0113-2304-10 | 00113230410 | 1 BOTTLE in 1 CARTON (0113-2304-10) > 30 mL in 1 BOTTLE | 1 bottle | 1991-07-29 | 0000-00-00 | No | No | Current |