NDC 13985-378 - BLOAT TREATMENT
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
- 13985-378
- Package NDCs from labels
- 13985-378-12
- Manufacturer
- MWI/VetOne
- Effective date
- 2018-03-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| BLOAT TREATMENT - MWI/VetOne | MWI/VetOne | 2018-03-29 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 13985-378-12 | BLOAT TREATMENT | 354.84 mL in 1 BOTTLE | EMULSION | 354.84 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| DOCUSATE SODIUM | ACTIVE INGREDIENT | F05Q2T2JA0 | BLOAT TREATMENT (DOCUSATE SODIUM) EMULSION [MWI/VETONE] | 1 | |
| DOCUSATE | ACTIVE MOIETY | M7P27195AG | BLOAT TREATMENT (DOCUSATE SODIUM) EMULSION [MWI/VETONE] | 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 |
|---|---|---|---|---|---|---|
| Topcare Stool Softener | DOCUSATE SODIUM | TopCo Associates, LLC | 6f4fddda-4129-4087-b0e4-ababc5558484 | 2021-02-19 | Warnings | F05Q2T2JA0 |
| Stool Softener | DOCUSATE SODIUM | Allegiant Health | 30c9ff75-cee4-4632-86fd-acfdf5ee85af | 2020-10-27 | Warnings | F05Q2T2JA0 |
| Stool Softener | MARC GLASSMAN | Marc Glassman, Inc. | 909cd222-d836-416f-aa7d-deb4a0c5a560 | 2020-09-08 | Warnings | F05Q2T2JA0 |
| STOOL SOFTENING SENNA LAXATIVE | SENNOSIDES 8.6 MG - DOCUSATE SODIUM 50 MG | TARGET CORPORATION | 7c74bd91-6687-2b89-e053-2a91aa0ad6b8 | 2019-02-28 | Warnings | F05Q2T2JA0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.