NDC 86193-4666 - FS IoBlend 10
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
- 86193-4666
- Package NDCs from labels
- 86193-4666-1
- Manufacturer
- Genex Cooperative, Inc. | ProActive Solutions USA, LLC
- Effective date
- 2024-04-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FS IoBlend 10 - Genex Cooperative, Inc. | ProActive Solutions USA, LLC | Genex Cooperative, Inc. | ProActive Solutions USA, LLC | 2024-04-04 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86193-4666-1 | FS IoBlend 10 | 1192.20 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK | SOLUTION | 1192.20 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 86193-4666 | FS IOBLEND 10 (IODINE) SOLUTION [GENEX COOPERATIVE, INC.] | 2 | 1 package rows | 20240405_fde4445f-ad1a-4a72-b59c-b46ca380c6f5.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.