NDC 54973-3379-01 - 4 Kids Cold and Cough Day and Night Grape Flavor
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
- 54973-3379
- Requested NDC
- 54973-3379-01
- Package NDCs from labels
- 54973-3379-1, 54973-3379-01
- Manufacturer
- Hyland's Inc.
- Effective date
- 2025-12-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hyland's Kids Cold 'n Cough Day & Night Combo Pack Grape Flavor | Hyland's Inc. | 2025-12-19 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54973-3243-1 | 4 Kids Cold and Cough Day and Night Grape Flavor | 1 in 1 CARTON | LIQUID | 6 [hp_X] in 1mL | 11 | |
| 54973-3243-1 | 4 Kids Cold and Cough Day and Night Grape Flavor | 118 mL in 1 BOTTLE, PLASTIC | LIQUID | 118 mL | 6 [hp_X] in 1mL | 11 |
| 54973-3377-1 | 4 Kids Cold and Cough Day and Night Grape Flavor | 1 in 1 CARTON | LIQUID | 6 [hp_X] in 1mL | 11 | |
| 54973-3377-1 | 4 Kids Cold and Cough Day and Night Grape Flavor | 118 mL in 1 BOTTLE, PLASTIC | LIQUID | 118 mL | 12 [hp_X] in 1mL | 11 |
| 54973-3379-1 | 4 Kids Cold and Cough Day and Night Grape Flavor | 1 in 1 CARTON | KIT | 1 | 11 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 54973-3379 | 4 KIDS COLD AND COUGH DAY AND NIGHT GRAPE FLAVOR (ONION,ANEMONE PULSATILLA, PHOSPHORUS, GOLDENSEAL, CALCIUM SULFIDE, SODIUM CHLORIDE, SULFUR, MATRICARIA CHAMOMILLA AND ARABICA COFFEE BEAN) KIT [HYLAND'S INC.] | 7 | Current NDC, Legacy NDC, 5 package rows | 20250502_79f26bb5-15ad-e40a-e053-2991aa0aaab3.zip |
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.