NDC 54973-3375-01 - 4 Kids Cold and Cough Nighttime
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
- 54973-3375
- Requested NDC
- 54973-3375-01
- Package NDCs from labels
- 54973-3375-1, 54973-3375-2, 54973-3375-3, 54973-3375-01
- Manufacturer
- Hyland's Consumer Health Inc. | Hyland's Inc.
- Effective date
- 2025-02-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hyland's Naturals Kids Cold & Cough Nighttime | Hyland's Consumer Health Inc. | Hyland's Inc. | 2025-02-06 | 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 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54973-3375-1 | 4 Kids Cold and Cough Nighttime | 1 in 1 CARTON | LIQUID | 1 | 11 | |
| 54973-3375-1 | 4 Kids Cold and Cough Nighttime | 118 mL in 1 BOTTLE, PLASTIC | LIQUID | 118 | 11 | |
| 54973-3375-2 | 4 Kids Cold and Cough Nighttime | 5 mL in 1 PACKET | LIQUID | 5 | 11 | |
| 54973-3375-3 | 4 Kids Cold and Cough Nighttime | 1 in 1 CARTON | LIQUID | 1 | 11 | |
| 54973-3375-3 | 4 Kids Cold and Cough Nighttime | 148 mL in 1 BOTTLE, PLASTIC | LIQUID | 148 | 11 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 54973-3375 | 4 KIDS COLD AND COUGH NIGHTTIME (ONION, CALCIUM SULFIDE, SODIUM CHLORIDE, ANEMONE PULSATILLA, ARABICA COFFEE BEAN, MATRICARIA CHAMOMILLA, SULFUR, PHOSPHORUS AND GOLDENSEAL) LIQUID [HYLAND'S CONSUMER HEALTH INC.] | 11 | Current NDC, Legacy NDC, 5 package rows | 20250209_71e93027-33c9-6147-e053-2a95a90aaa09.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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| Fendall 2000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a1d07e-0006-0c75-e063-6394a90a7acc | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 1000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a2f4da-bb1e-8ead-e063-6394a90af72e | 2026-07-02 | Warnings | 059QF0KO0R |
| Sterile Eyesaline Eyewash | STERILE EYESALINE EYEWASH | Protective Industrial Products, Inc. | 55a290e8-8310-8be4-e063-6394a90abdce | 2026-07-02 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Protective Industrial Products, Inc. | 55a261c2-725d-6765-e063-6294a90a3260 | 2026-07-02 | Warnings | 059QF0KO0R |
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| Magnilife Pain Relieving Foot | APIS MELLIFERA, LEONTOPODIUM NIVALE SUBSP. ALPINUM WHOLE, SULFUR | The Magni Group, Inc. | 626e52cc-3031-47a4-8e31-f5ae51b51846 | 2026-07-01 | Warnings | 70FD1KFU70 |
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| NebuClear MD Saline | NEBUCLEAR MD SALINE | Blue Echo Care LLC | 55806cb8-cf92-c4e5-e063-6394a90aaa2d | 2026-06-30 | Warnings | 451W47IQ8X |
| NebuClear MD Saline | NEBUCLEAR MD SALINE | Blue Echo Care LLC | 5581d8e5-4105-e9da-e063-6394a90a316e | 2026-06-30 | Warnings | 451W47IQ8X |
| Glycerin | GLYCERIN | Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd | 552d9018-cc7d-7e1a-e063-6294a90a3322 | 2026-06-26 | Warnings | PDC6A3C0OX |
| Glycerin | GLYCERIN | Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd | 552e16b9-f46a-7838-e063-6394a90ab8aa | 2026-06-26 | Warnings | PDC6A3C0OX |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.