NDC 70069-692-01 - Zinc sulfate
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
- 70069-692
- Requested NDC
- 70069-692-01
- Package NDCs from labels
- 70069-692-01, 70069-692-25
- Manufacturer
- Somerset Therapeutics, LLC | Somerset Therapeutics Limited
- Effective date
- 2024-07-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Zinc sulfate - Somerset Therapeutics, LLC | Somerset Therapeutics Limited | Somerset Therapeutics, LLC | Somerset Therapeutics Limited | 2024-07-18 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70069-692-01 | Zinc sulfate | 10 mL in 1 VIAL | SOLUTION | 10 | 3 | |
| 70069-692-25 | Zinc sulfate | 25 in 1 CARTON | SOLUTION | 25 | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70069-692-01 | ML - Milliliter | 70069-692 | 20926a1c-550d-40eb-91cb-25b766a5dd7c | 1 | 2024-08-12 |
| 70069-692-25 | ML - Milliliter | 70069-692 | 99611e07-8776-4a45-8b2f-d5b8c8e4919f | 1 | 2024-08-12 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Bio Rock Water | ROCK WATER | BioActive Nutritional, Inc. | 178bd16d-0d4f-49d8-866b-8ab3a3c6889d | 2018-07-30 | Warnings | 059QF0KO0R |
| Trauma plus Gel | CALENDULA OFFICINALIS, ARNICA MONTANA, HYPERICUM PERFORATUM, SYMPHYTUM OFFICINALE, BELLIS PERENNIS, LEDUM PALUSTRE, SULPHURICUM ACIDUM, CALCAREA FLUORICA, FERRUM PHOSPHORICUM, RHUS TOX, RUTA GRAVEOLENS, NATRUM SULPHURICUM | Energique, Inc. | 6da04ff9-4088-427c-9757-36092c8f7585 | 2018-02-08 | Warnings | O40UQP6WCF |
| Sterile Water | WATER | Baxter Healthcare Corporation | ef3e79c5-3f58-4b36-a296-64b7d9a651c1 | 2017-10-17 | Warnings, Adverse reactions | 059QF0KO0R |
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.