NDC 17433-9877-05 - ENEMEEZ Plus
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
- 17433-9877
- Requested NDC
- 17433-9877-05
- Package NDCs from labels
- 17433-9877-0, 17433-9877-3, 17433-9877-6, 17433-9877-5, 17433-9877-7, 17433-9877-2, 17433-9877-1, 17433-9877-4, 17433-9877-05
- 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 Plus - 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 |
|---|---|---|---|---|---|---|
| 17433-9877-0 | ENEMEEZ Plus | 5 mL in 1 TUBE | LIQUID | 5 | 22 | |
| 17433-9877-1 | ENEMEEZ Plus | 1 in 1 CONTAINER | LIQUID | 1 | 22 | |
| 17433-9877-2 | ENEMEEZ Plus | 2 in 1 CONTAINER | LIQUID | 2 | 22 | |
| 17433-9877-3 | ENEMEEZ Plus | 30 in 1 CONTAINER | LIQUID | 30 | 22 | |
| 17433-9877-5 | ENEMEEZ Plus | 5 in 1 CONTAINER | LIQUID | 5 | 22 | |
| 17433-9877-6 | ENEMEEZ Plus | 35 in 1 CONTAINER | LIQUID | 35 | 22 | |
| 17433-9877-7 | ENEMEEZ Plus | 6 in 1 CONTAINER | LIQUID | 6 | 22 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17433-9877 | ENEMEEZ PLUS (DOCUSATE SODIUM AND BENZOCAINE) LIQUID [QUEST PRODUCTS, LLC] | 20 | Current NDC, Legacy NDC, 7 package rows | 20250216_1670ca59-7275-4ac6-bef4-674a7b24c7b3.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 17433-9877-0 | ML - Milliliter | 17433-9877 | 2e9b0ac6-919d-4fe2-a8ba-a2b8c95ed351 | 1 | 2018-05-09 |
| 17433-9877-2 | ML - Milliliter | 17433-9877 | 0f3c3df0-f564-4e9a-9b9e-7083e97ea8fe | 1 | 2025-09-12 |
| 17433-9877-3 | ML - Milliliter | 17433-9877 | 53354c2d-cba7-4902-8a17-9cd8f7ede81b | 1 | 2013-02-13 |
| 17433-9877-5 | ML - Milliliter | 17433-9877 | 7b0c7f3e-bcf2-4dd1-b6d2-bb54d55b0209 | 1 | 2022-05-04 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| BENZOCAINE | ACTIVE INGREDIENT | U3RSY48JW5 | ENEMEEZ PLUS (DOCUSATE SODIUM AND BENZOCAINE) LIQUID [ENEMEEZ INC. DBA SUMMIT PHARMACEUTICALS] | 3 | |
| DOCUSATE SODIUM | ACTIVE INGREDIENT | F05Q2T2JA0 | ENEMEEZ PLUS (DOCUSATE SODIUM AND BENZOCAINE) LIQUID [ENEMEEZ INC. DBA SUMMIT PHARMACEUTICALS] | 3 | |
| BENZOCAINE | ACTIVE MOIETY | U3RSY48JW5 | ENEMEEZ PLUS (DOCUSATE SODIUM AND BENZOCAINE) LIQUID [ENEMEEZ INC. DBA SUMMIT PHARMACEUTICALS] | 3 | |
| DOCUSATE | ACTIVE MOIETY | M7P27195AG | ENEMEEZ PLUS (DOCUSATE SODIUM AND BENZOCAINE) LIQUID [ENEMEEZ INC. DBA SUMMIT PHARMACEUTICALS] | 3 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | ENEMEEZ PLUS (DOCUSATE SODIUM AND BENZOCAINE) LIQUID [ENEMEEZ INC. DBA SUMMIT PHARMACEUTICALS] | 3 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | ENEMEEZ PLUS (DOCUSATE SODIUM AND BENZOCAINE) 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| SENOKOT | STANDARDIZED SENNA | A-S Medication Solutions | 0c6e6bdd-9f49-4550-b60a-8f58b7c0f090 | 2026-09-09 | Warnings | M007 |
| Bisacodyl | BISACODYL | KROGER COMPANY | a13a8eec-3652-8c57-e053-2995a90aaebf | 2026-09-09 | Warnings | M007 |
| Leader Eye Drops Redness Relief | GLYCERIN, NAPHAZOLINE HYDROCHLORIDE | Cardinal Health | aee4bbe2-4f11-4c54-be8b-df48b3ba4f3a | 2026-09-09 | Warnings | PDC6A3C0OX |
| Stool Softener Laxative | DOCUSATE SODIUM | TARGET Corporation | 4180a35b-cc50-46ae-a100-99bb218c10ff | 2026-09-09 | Warnings | M007 F05Q2T2JA0 |
| Hemorrhoidal | GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM | Rite Aid Corporation | 407c78ca-6fee-4ed6-b61b-711ec049c86e | 2026-09-09 | Warnings | PDC6A3C0OX |
| fiber laxative | PSYLLIUM HUSK | Raritan Pharmaceuticals Inc | 22e927bd-5734-424e-8870-1aaa18f1265e | 2026-09-08 | Warnings | M007 |
| Clear Eyes Nighttime | GLYCERIN | Prestige Brands Holdings, Inc. | af75e2f7-81dd-43e0-a390-b52bbfbebf62 | 2026-09-08 | Warnings | PDC6A3C0OX |
| DRx Choice Fiber Therapy | METHYLCELLULOSE | RARITAN PHARMACEUTICALS INC | 5e5749f7-074e-4bbc-9f33-5090e603fdb4 | 2026-09-08 | Warnings | M007 |
| Bisacodyl Stimulant Laxative | BISACODYL | Raritan Pharmaceuticals Inc | b99c1a6d-3034-4822-8540-210179c06857 | 2026-09-08 | Warnings | M007 |
| Daily Fiber Sugar Free | PSYLLIUM HUSK | Raritan Pharmaceuticals Inc | 9c4c41d8-a2d5-4168-9e97-9f9d47fc5e63 | 2026-09-08 | Warnings | M007 |
| DRx Choice Fiber Therapy | METHYLCELLULOSE | RARITAN PHARMACEUTICALS INC | 56c7f197-f01a-4611-a761-cda18da6eed0 | 2026-09-08 | Warnings | M007 |
| Sting Relief Pad | BENZOCAINE, ISOPROPYL ALCOHOL CLOTH | JINHUA JINGDI MEDICAL SUPPLIES CO., LTD | 57ccc28b-5f5f-30ec-e063-6294a90a081c | 2026-09-07 | Warnings | U3RSY48JW5 |
| Sennosides 8.6 mg | SENNOSIDES | Morepen Bio Inc | 562c9f11-0ba1-011d-e063-6394a90a604a | 2026-09-05 | Warnings | M007 |
| Epsom Salt | MAGNESIUM SULFATE | Target Corporation | 87f98e6c-a3a1-4ca5-bd56-977e38f48914 | 2026-09-04 | Warnings, Adverse reactions | M007 |
| Hemorrhoidal | GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM | CVS Pharmacy | 3167c918-a7d3-46a1-a85b-64f9c22916f2 | 2026-09-04 | Warnings | PDC6A3C0OX |
| SurviveX Sting Relief | STING RELIEF WIPE | Changzhou Maokang Medical Products Co., Ltd. | 5a83b1f1-c8dc-cf07-e063-6394a90a20ca | 2026-09-03 | Warnings | U3RSY48JW5 |
| Kroger Stool Softener Fruit Punch | DOCUSATE SODIUM | KROGER COMPANY | b86f8f3d-594e-466c-854a-b8bff9f7a0b8 | 2026-09-02 | Warnings | M007 F05Q2T2JA0 |
| Oil | MINERAL OIL | Atlantic Biologicals Corp. | 5a82197b-281d-76c0-e063-6294a90a5746 | 2026-09-02 | Warnings, Adverse reactions | M007 |
| Kroger Senna Laxative Regular Strength | SENNOSIDES | KROGER COMPANY | dbb040bb-21f9-43e8-9705-689aeee4d04c | 2026-09-01 | Warnings | M007 |
| Stimulant Laxative Plus Stool Softener | DOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MG | Preferred Pharmaceuticals, Inc. | b25b8a28-5e00-4a20-9ca3-7ed494fc4540 | 2026-09-01 | Warnings | F05Q2T2JA0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.