NDC 86193-4160 - FS EDX-1000
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
- 86193-4160
- Package NDCs from labels
- 86193-4160-1
- Manufacturer
- Genex Cooperative, Inc. | ProActive Solutions USA, LLC
- Effective date
- 2024-01-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FS EDX-1000 - Genex Cooperative, Inc. | ProActive Solutions USA, LLC | Genex Cooperative, Inc. | ProActive Solutions USA, LLC | 2024-01-12 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86193-4160-1 | FS EDX-1000 | 1068.40 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK | LIQUID | 1068.40 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 86193-4160 | FS EDX-1000 (IODINE) LIQUID [GENEX COOPERATIVE, INC.] | 1 | 1 package rows | 20240113_d66926bd-551a-411d-832b-e9a79186f4df.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Bio Iodine | IODIUM | BioActive Nutritional, Inc. | 69be0ca4-99b7-4de0-b4f2-5723b1f1a7da | 2016-08-11 | Warnings | 9679TC07X4 |
| Thyrotox | CHONDRUS CRISPUS, FUCUS VESICULOSUS, THYROIDINUM, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, IODIUM, KALI CARBONICUM, PHOSPHORUS, PULSATILLA (VULGARIS), SILICEA | BioActive Nutritional, Inc. | e229a260-13f3-4136-b325-9a8954f8a327 | 2016-08-10 | Warnings | 9679TC07X4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.