NDC 29983-1063 - Genesis 110 SPRA
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
- 29983-1063
- Package NDCs from labels
- 29983-1063-9, 29983-1063-8
- Manufacturer
- IBA | Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.
- Effective date
- 2025-11-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Genesis 110 SPRAY | IBA | Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. | 2025-11-26 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 29983-1063-8 | Genesis 110 SPRA | 216.25 kg in 1 DRUM | LIQUID | 216.25 | 10 | |
| 29983-1063-9 | Genesis 110 SPRA | 1040.99 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK | LIQUID | 1040.99 | 10 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 29983-1063 | GENESIS 110 SPRA (IODINE) LIQUID [IBA] | 9 | 2 package rows | 20241108_a6e8690d-773d-44dc-a43f-d4fbc28de82e.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.