NDC 54973-3075-01 - Cold and Cough 4 Kids
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
- 54973-3075
- Requested NDC
- 54973-3075-01
- Package NDCs from labels
- 54973-3075-1, 54973-3075-2, 54973-3075-3, 54973-3075-01
- Manufacturer
- Hyland's Inc. | Applied Laboratories, Inc.
- Effective date
- 2025-10-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hyland’s Kids Cough & Cold Daytime | Hyland's Inc. | Applied Laboratories, Inc. | 2025-10-29 | HUMAN OTC DRUG LABEL |
| Hyland's Naturals Kids Cold 'n Cough Combo Pack | Hyland’s Inc. | Hyland's Inc. | 2023-09-27 | HUMAN OTC DRUG LABEL |
| 4 Kids Cold 'n Cough Day & Night Value Pack | Hylands Inc. | Standard Homeopathic Company | LGM Pharma Solutions, LLC | 2021-05-28 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54973-3075-1 | Cold and Cough 4 Kids | 118 mL in 1 BOTTLE, PLASTIC | LIQUID | 118 | 12 | |
| 54973-3075-2 | Cold and Cough 4 Kids | 1 in 1 CARTON | LIQUID | 1 | 12 | |
| 54973-3075-2 | Cold and Cough 4 Kids | 19.8 mL in 1 BOTTLE, PLASTIC | LIQUID | 19.8 | 12 | |
| 54973-3075-3 | Cold and Cough 4 Kids | 5 mL in 1 POUCH | LIQUID | 5 | 12 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 54973-3075 | COLD AND COUGH 4 KIDS (ONION, CALCIUM SULFIDE, SODIUM CHLORIDE, PHOSPHORUS, PULSATILLA VULGARIS, SULFUR, AND GOLDENSEAL) LIQUID [HYLAND'S INC.] | 10 | Current NDC, Legacy NDC, 4 package rows | 20230803_e06599ca-fc94-4b2c-829e-f3d4ec866ed6.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.