NDC 29983-1049 - Genesis 52
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
- 29983-1049
- Package NDCs from labels
- 29983-1049-8, 29983-1049-9
- 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 52 | 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 |
|---|---|---|---|---|---|---|
| 29983-1049-8 | Genesis 52 | 210.56 kg in 1 DRUM | LIQUID | 210.56 | 10 | |
| 29983-1049-9 | Genesis 52 | 1052.78 kg in 1 CONTAINER | LIQUID | 1052.78 | 10 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 29983-1049 | GENESIS 52 (TEAT DIP) LIQUID [IBA] | 9 | 2 package rows | 20241107_a417ef1e-3c7b-4015-95b0-90188734dca7.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| IODINE | ACTIVE INGREDIENT | 9679TC07X4 | GENESIS 52 (TEAT DIP) LIQUID [IBA] | 1 | |
| IODINE | ACTIVE MOIETY | 9679TC07X4 | GENESIS 52 (TEAT DIP) LIQUID [IBA] | 1 | |
| C10-16 PARETH-1 | INACTIVE INGREDIENT | 3Y76363WPB | GENESIS 52 (TEAT DIP) LIQUID [IBA] | 1 | |
| CITRIC ACID MONOHYDRATE | INACTIVE INGREDIENT | 2968PHW8QP | GENESIS 52 (TEAT DIP) LIQUID [IBA] | 1 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | GENESIS 52 (TEAT DIP) LIQUID [IBA] | 1 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | GENESIS 52 (TEAT DIP) LIQUID [IBA] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | GENESIS 52 (TEAT DIP) LIQUID [IBA] | 1 |
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.