NDC 29983-0052 - ASCEND
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
- 29983-0052
- Package NDCs from labels
- 29983-0052-1, 29983-0052-4, 29983-0052-6, 29983-0052-7, 29983-0052-8
- Manufacturer
- IBA
- Effective date
- 2022-07-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ASCEND - IBA | IBA | 2022-07-19 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 29983-0052-1 | ASCEND | 3.78 L in 1 BOTTLE, PLASTIC | SOLUTION | 3.78 | 2 | |
| 29983-0052-4 | ASCEND | 18.9 L in 1 DRUM | SOLUTION | 18.9 | 2 | |
| 29983-0052-6 | ASCEND | 56.7 L in 1 DRUM | SOLUTION | 56.7 | 2 | |
| 29983-0052-7 | ASCEND | 113.4 L in 1 DRUM | SOLUTION | 113.4 | 2 | |
| 29983-0052-8 | ASCEND | 207.9 L in 1 DRUM | SOLUTION | 207.9 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 29983-0052 | ASCEND (IODINE) SOLUTION [IBA] | 2 | 5 package rows | 20220721_1a8d09ec-cc62-414a-ad76-eaf45e595a8c.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.