NDC 50845-0282-01 - Tension Headache
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
- 50845-0282
- Requested NDC
- 50845-0282-01
- Package NDCs from labels
- 50845-0282-1, 50845-0282-2, 50845-0282-01
- Manufacturer
- Liddell Laboratories, Inc. | Apotheca Company
- Effective date
- 2025-11-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Tension Headache - Liddell Laboratories, Inc. | Apotheca Company | Liddell Laboratories, Inc. | Apotheca Company | 2025-11-20 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50845-0282-1 | Tension Headache | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 2 | |
| 50845-0282-2 | Tension Headache | 1 in 1 CARTON | SPRAY | 1 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50845-0282 | TENSION HEADACHE (ACONITUM NAPELLUS, CARDUUS MARIANUS, COFFEA CRUDA, DIOSCOREA VILLOSA, GELSEMIUM SEMPERVIRENS, GNAPHALIUM POLYCEPHALUM, IRIS VERSICOLOR, PASSIFLORA INCARNATA, STELLARIA MEDIA, VERBASCUM THAPSUS) SPRAY [LIDDELL LABORATORIES, INC.] | 1 | Current NDC, 2 package rows | 20250202_897a3348-4d9d-4f74-a330-d6492baa4d03.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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| HAND SANITIZER STRAWBERRY FIZZ | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 322e3045-14dc-ac2e-e063-6394a90a9b8a | 2025-06-29 | Warnings | 3K9958V90M |
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| HAND SANITIZER | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 38b87b19-7663-d5c5-e063-6294a90a9e87 | 2025-06-29 | Warnings | 3K9958V90M |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.