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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.