NDC 0031-2251 - Dimetapp Paediatric
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0031-2251
- Package NDCs from labels
- 0031-2251-12, 0031-2251-04, 0031-2251-05
- Manufacturer
- Haleon US Holdings LLC
- Effective date
- 2024-04-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dimetapp Paediatric - Haleon US Holdings LLC | Haleon US Holdings LLC | 2024-04-24 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0031-2251-04 | Dimetapp Paediatric | 118 mL in 1 BOTTLE | ELIXIR | 118 | 7 | |
| 0031-2251-04 | Dimetapp Paediatric | 1 in 1 CARTON | ELIXIR | 1 | 7 | |
| 0031-2251-05 | Dimetapp Paediatric | 1 in 1 CARTON | ELIXIR | 1 | 7 | |
| 0031-2251-05 | Dimetapp Paediatric | 118 mL in 1 BOTTLE | ELIXIR | 118 | 7 | |
| 0031-2251-12 | Dimetapp Paediatric | 1 in 1 CARTON | ELIXIR | 1 | 7 | |
| 0031-2251-12 | Dimetapp Paediatric | 118 mL in 1 BOTTLE | ELIXIR | 118 | 7 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.