NDC 50845-0263-01 - Sinus Congestion 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
- 50845-0263
- Requested NDC
- 50845-0263-01
- Package NDCs from labels
- 50845-0263-1, 50845-0263-2, 50845-0263-01
- Manufacturer
- Liddell Laboratories, Inc. | Apotheca Company
- Effective date
- 2024-11-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Sinus Congestion Headache - Liddell Laboratories, Inc. | Apotheca Company | Liddell Laboratories, Inc. | Apotheca Company | 2024-11-04 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50845-0263-2 | 2024-11-04 | C162847 | 48780-1 | f386c64a-2ba8-0266-e053-dadaa90a7c1a | DRUG FACTS: |
| 50845-0263-2 | 2023-01-30 | C162847 | 48780-1 | f386c64a-2ba8-0266-e053-dadaa90a7c1a | DRUG FACTS: |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50845-0263-1 | Sinus Congestion Headache | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 3 | |
| 50845-0263-2 | Sinus Congestion Headache | 1 in 1 PACKAGE | SPRAY | 1 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50845-0263 | SINUS CONGESTION HEADACHE (ANTIMONIUM TARTARICUM, ASAFOETIDA, BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), EUPATORIUM PERFOLIATUM, EUPHORBIA PILULIFERA, HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, IODIUM, KALI BICHROMICUM, LACHESIS MUTUS, MAGNESIA CARBONICA, MUCOSA NASALIS SUIS, PULSATILLA (PRATENSIS), PYROGENIUM, SILICEA, TEUCRIUM MARUM) SPRAY [LIDDELL LABORATORIES, INC.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20241105_debc7747-8664-4598-a862-e295188c4fca.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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| Vermex 6016 | VERMEX | Professional Complementary Health Formulas | a8a70546-ae5d-4524-b6bc-3dc0a989faec | 2026-01-08 | Warnings | 10464S0TAA |
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| First Chakra (Root) 7301 | FIRST CHAKRA (ROOT) | Professional Complementary Health Formulas | 61eb1bbe-6675-4369-b852-18975e6b08c7 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Second Chakra (Sacral) 7302 | SECOND CHAKRA (SACRAL) | Professional Complementary Health Formulas | ea8a69d3-66fc-4b21-bfdd-c207dd293589 | 2026-01-08 | Warnings | ETJ7Z6XBU4 VSW71SS07I |
| Silicea 8012 | SILICEA | Professional Complementary Health Formulas | a2a1eae8-24c8-44dd-9b9d-1826fa716433 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
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| Intestine Drops 5009 | INTESTINE DROPS | Professional Complementary Health Formulas | 51298670-06bb-4b17-a7e5-3efd91717c1a | 2026-01-08 | Warnings | ZW3Z11D0JV |
| Low Bacterial Nosode 4022 | LOW BACTERIAL NOSODE | Professional Complementary Health Formulas | 896b752f-3322-4b17-9480-fe4865cca973 | 2026-01-08 | Warnings | 29SUH5R3HU |
| Thymus Drops 5027 | THYMUS DROPS | Professional Complementary Health Formulas | 8d7c42f7-02ae-4992-986f-4743151ad3bb | 2026-01-08 | Warnings | ETJ7Z6XBU4 VSW71SS07I 1MBW07J51Q |
| Drosera Combination 9221 | DROSERA COMBINATION | Professional Complementary Health Formulas | 5ae94676-2b6e-4888-8691-a8aa9a6c59c9 | 2026-01-08 | Warnings | VSW71SS07I |
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| Causticum Combination 9253 | CAUSTICUM COMBINATION | Professional Complementary Health Formulas | 82b1a723-63e6-41b4-9940-a984dd719c87 | 2026-01-08 | Warnings | 1MBW07J51Q |
| Rose Quartz 8142 | ROSE QUARTZ | Professional Complementary Health Formulas | 898cd57d-8656-457d-92ff-5b4ea1357800 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
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| PMS Drops 2124 | PMS DROPS | Professional Complementary Health Formulas | d05bfbbe-d19d-4fd5-8679-bf17d0b61840 | 2026-01-08 | Warnings | VSW71SS07I |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.