NDC 79903-412 - Childrens Cough and Congestion, Childrens Cold and Cough Day, Night
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
- 79903-412
- Package NDCs from labels
- 79903-412-08
- Manufacturer
- WALMART INC. | LNK International, Inc.
- Effective date
- 2026-05-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Equate 44-019020 | WALMART INC. | LNK International, Inc. | 2026-05-19 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79903-412-08 | Childrens Cough and Congestion, Childrens Cold and CoughDay, Night | 237 mL in 1 BOTTLE, PLASTIC | SOLUTION | 237 mL | 100 mg in 15mL | 1 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.