NDC 79481-0336-01 - Calamine
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
- 79481-0336
- Requested NDC
- 79481-0336-01
- Package NDCs from labels
- 79481-0336-1, 79481-0336-01
- Manufacturer
- Meijer, Inc. | Nice-Pak Products, LLC
- Effective date
- 2026-02-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Calamine - Meijer, Inc. | Nice-Pak Products, LLC | Meijer, Inc. | Nice-Pak Products, LLC | 2026-02-19 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-0336-1 | Calamine | 177 mL in 1 BOTTLE, PLASTIC | LOTION | 177 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79481-0336 | CALAMINE (CALAMINE, PRAMOXINE HCL) LOTION [MEIJER DISTRIBUTION, INC] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241114_6b369ef2-fd54-4931-a9eb-0fb42834c2ef.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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| pramosone | HYDROCORTISONE ACETATE AND PRAMOXINE HYDROCHLORIDE | Legacy Pharma USA Inc. | 4d4fb647-0304-f4ac-e063-6294a90af513 | 2026-03-18 | Adverse reactions | 88AYB867L5 |
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| Advanced Bed Sore Wound Healing | ALLANTOIN | Yantai Aien Biotechnology Co., Ltd. | 4d589c18-e597-355a-e063-6394a90a4243 | 2026-03-18 | Warnings | M016 |
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| Powder | TITANIUM DIOXIDE | Oxygen Development LLC | 4d3a0a92-b0de-a1ea-e063-6294a90a8508 | 2026-03-17 | Warnings | 1K09F3G675 |
| MediChoice Barrier | DIMETHICONE | O&M HALYARD, INC. | 115c2a2f-d68a-316a-e063-6394a90a2716 | 2026-03-17 | Warnings | M016 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.