NDC 17433-9876-01 - ENEMEEZ
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
- 17433-9876
- Requested NDC
- 17433-9876-01
- Package NDCs from labels
- 17433-9876-0, 17433-9876-3, 17433-9876-9, 17433-9876-5, 17433-9876-6, 17433-9876-2, 17433-9876-1, 17433-9876-4, 17433-9876-01
- Manufacturer
- Quest Products, LLC | Enemeez LLC DBA Summit Pharmaceuticals
- Effective date
- 2026-06-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ENEMEEZ - Quest Products, LLC | Enemeez LLC DBA Summit Pharmaceuticals | Quest Products, LLC | Enemeez LLC DBA Summit Pharmaceuticals | 2026-06-30 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17433-9876-0 | ENEMEEZ | 5 mL in 1 TUBE | LIQUID | 5 | 19 | |
| 17433-9876-1 | ENEMEEZ | 1 in 1 CONTAINER | LIQUID | 1 | 19 | |
| 17433-9876-2 | ENEMEEZ | 2 in 1 CONTAINER | LIQUID | 2 | 19 | |
| 17433-9876-3 | ENEMEEZ | 30 in 1 CONTAINER | LIQUID | 30 | 19 | |
| 17433-9876-5 | ENEMEEZ | 5 in 1 CONTAINER | LIQUID | 5 | 19 | |
| 17433-9876-6 | ENEMEEZ | 6 in 1 CONTAINER | LIQUID | 6 | 19 | |
| 17433-9876-9 | ENEMEEZ | 35 in 1 CONTAINER | LIQUID | 35 | 19 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17433-9876 | ENEMEEZ (DOCUSATE SODIUM) LIQUID [QUEST PRODUCTS, LLC] | 17 | Current NDC, Legacy NDC, 7 package rows | 20250216_0b06445d-0839-497e-bdff-e0fe224a7738.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 17433-9876-0 | ML - Milliliter | 17433-9876 | 4408cdb5-7d28-4c34-8651-717075a70e49 | 1 | 2018-05-09 |
| 17433-9876-2 | ML - Milliliter | 17433-9876 | fe479dae-1bb2-489e-b119-6607a33cad99 | 1 | 2025-09-12 |
| 17433-9876-3 | ML - Milliliter | 17433-9876 | c1a7690a-b611-428d-8bb4-2187e4a2adc8 | 1 | 2013-02-13 |
| 17433-9876-5 | ML - Milliliter | 17433-9876 | 944b4aa2-9468-4755-856d-4c50bf4c7348 | 1 | 2022-05-04 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| DOCUSATE SODIUM | ACTIVE INGREDIENT | F05Q2T2JA0 | ENEMEEZ (DOCUSATE SODIUM) LIQUID [ENEMEEZ INC. DBA SUMMIT PHARMACEUTICALS] | 3 | |
| DOCUSATE | ACTIVE MOIETY | M7P27195AG | ENEMEEZ (DOCUSATE SODIUM) LIQUID [ENEMEEZ INC. DBA SUMMIT PHARMACEUTICALS] | 3 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | ENEMEEZ (DOCUSATE SODIUM) LIQUID [ENEMEEZ INC. DBA SUMMIT PHARMACEUTICALS] | 3 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | ENEMEEZ (DOCUSATE SODIUM) LIQUID [ENEMEEZ INC. DBA SUMMIT PHARMACEUTICALS] | 3 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.