NDC 17307-3190 - AlphaPro
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
- 17307-3190
- Package NDCs from labels
- 17307-3190-1, 17307-3190-2, 17307-3190-3, 17307-3190-4
- Manufacturer
- AgroChem USA, LLC
- Effective date
- 2024-11-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Iodine Solution - AgroChem USA, LLC | AgroChem USA, LLC | 2024-11-11 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17307-3190-1 | AlphaPro | 19 kg in 1 CONTAINER | SOLUTION | 19 | 2 | |
| 17307-3190-2 | AlphaPro | 57 kg in 1 DRUM | SOLUTION | 57 | 2 | |
| 17307-3190-3 | AlphaPro | 208 kg in 1 DRUM | SOLUTION | 208 | 2 | |
| 17307-3190-4 | AlphaPro | 1040 kg in 1 CONTAINER | SOLUTION | 1040 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17307-3190 | ALPHAPRO (IODINE SOLUTION) SOLUTION [AGROCHEM USA, LLC] | 2 | 4 package rows | 20241113_a903a919-d749-42e8-b48b-acdd2e1eadeb.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.