NDC 69367-234 - WestGel DHA
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
- 69367-234
- Package NDCs from labels
- 69367-234-30
- Manufacturer
- Westminster Pharmaceuticals, LLC
- Effective date
- 2023-07-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| WestGel DHA - Westminster Pharmaceuticals, LLC | Westminster Pharmaceuticals, LLC | 2023-07-14 | DIETARY SUPPLEMENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69367-234-30 | WestGel DHA | 3 in 1 CARTON | CAPSULE, LIQUID FILLED | 3 | 3 | |
| 69367-234-30 | WestGel DHA | 10 in 1 BLISTER PACK | CAPSULE, LIQUID FILLED | 10 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69367-234 | WESTGEL DHA (ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, D-, THIAMINE HYDROCHLORIDE, RIBOFLAVIN, NIACIN, PYRIDOXINE HYDROCHLORIDE, LEVOMEFOLATE MAGNESIUM, FOLIC ACID, CYANOCOBALAMIN, IRON PENTACARBONYL, POTASSIUM IODIDE, MAGNESIUM OXIDE, DOCONEXENT, AND ICOSAPENT) CAPSULE, LIQUID FILLED [WESTMINSTER PHARMACEUTICALS, LLC] | 3 | 2 package rows | 20230718_fc0dcc5f-7b0f-4f91-98d5-8d47a65eb294.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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.