nasal
- Product NDC
- 30142-303
- Requested package NDC
- 30142-303-10
- 11-digit product format
- 301420303
- Labeler code
- 30142
- Product ID
- 30142-303_c00797cf-292b-437d-8119-1645abb0f989
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxymetazoline hydrochloride
- Dosage form
- SPRAY
- Route
- NASAL
- Labeler
- Kroger Company
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-06-21
- Marketing end
- 0000-00-00
- Substance
- OXYMETAZOLINE HYDROCHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 30142-303 | 30142-303-10 | D | Discontinued by firm | 2026-10-16 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 30142-303-10 | 30142030310 | 1 BOTTLE, SPRAY in 1 CARTON (30142-303-10) > 30 mL in 1 BOTTLE, SPRAY | 2016-06-21 | 0000-00-00 | No | No | Current |