Home NDC 17433-9877-2 ENEMEEZ Plus
Product NDC 17433-9877
Requested package NDC 17433-9877-2
11-digit product format 174339877
Labeler code 17433
Product ID 17433-9877_557c260c-c8fb-da2f-e063-6294a90a5501
Type HUMAN OTC DRUG
Nonproprietary name docusate sodium and benzocaine
Dosage form LIQUID
Route RECTAL
Labeler Quest Products, LLC
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-06-15
Substance BENZOCAINE; DOCUSATE SODIUM
Active strength 20; 283 mg/5mL; mg/5mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base ENEMEEZ Plus
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 20 mg/5mL DOCUSATE SODIUM 283 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup F05Q2T2JA0 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1192984 Internal RxNorm lookup 1192986 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table 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
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.
Matched openFDA labels page 20 of 42 · 829 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join up and up fiber therapy PSYLLIUM HUSK TARGET CORPORATION 956c48f8-c705-4a86-9866-c68a48ddeb6c 2025-11-05 Warnings Exact identifier application number: M007 CEO-TWO LAXATIVE Beutlich Pharmaceuticals, LLC 08670636-5795-4db0-e063-6294a90afa4b 2025-11-05 Warnings Exact identifier application number: M007 up and up gentle laxative BISACODYL Target Corporation 4a29dc2b-b68f-471b-a84e-4a5096aa3748 2025-11-04 Warnings Exact identifier application number: M007 Target Fiber Laxative PSYLLIUM HUSK TARGET CORPORATION a581116a-392d-4ac3-ae15-4318506a7b2a 2025-11-04 Warnings Exact identifier application number: M007 up and up fiber therapy CALCIUM POLYCARBOPHIL Target Corporation. e5473950-06f4-4ea4-975b-3ac94957e776 2025-11-04 Warnings Exact identifier application number: M007 up and up fiber therapy Natural Fiber PSYLLIUM HUSK Target Corporation f8b1c831-6fd0-4a58-9726-4e0f986c8084 2025-11-04 Warnings Exact identifier application number: M007 OneLAX BISACODYL AKRON PHARMA INC be4eeb4d-df29-45dc-94ff-933e52c8b6f6 2025-11-03 Warnings Exact identifier application number: M007 Gentle Stool Softener DOCUSATE SODIUM WALGREEN COMPANY 169b33f9-e559-47bf-bbba-c7eda4762c7f 2025-10-31 Warnings Exact identifier application number: M007 Senna S DOCUSATE SODIUM, SENNOSIDES Walgreens 765bfd9b-7a21-4315-9add-cf13007722d5 2025-10-31 Warnings Exact identifier application number: M007 Gentle Stool Softener DOCUSATE SODIUM WALGREEN COMPANY 71b15339-2585-4fae-8445-6fbb4f0a378e 2025-10-31 Warnings Exact identifier application number: M007 Stool Softener Laxative DOCUSATE SODIUM Major Pharmaceuticals 97561cd4-63d9-44c2-a3a3-ec668a09a4ed 2025-10-31 Warnings Exact identifier application number: M007 Fiber Caplets CALCIUM POLYCARBOPHIL SAFEWAY 08e2e8b0-90b3-48d6-a72a-40688c74771a 2025-10-29 Warnings Exact identifier application number: M007 Glycerin GLYCERIN Chain Drug Marketing Association Inc. 424d91f0-ecf9-6d9b-e063-6394a90a8006 2025-10-29 Warnings Exact identifier application number: M007 Publix Laxative Maximum Strength CALCIUM SENNOSIDES PUBLIX SUPER MARKETS, INC 11112859-ef1e-4b37-9915-ba4d06a3f198 2025-10-28 Warnings Exact identifier application number: M007 Publix Stimulant Laxative BISACODYL PUBLIX SUPER MARKETS, INC 02e596a7-b8e5-4f55-9bc6-6d17e0fabda7 2025-10-28 Warnings Exact identifier application number: M007 PUBLIX PSYLLIUM HUSK PUBLIX SUPER MARKETS, INC 55f98d3f-f282-4f19-b373-0b59640d274d 2025-10-28 Warnings Exact identifier application number: M007 PUBLIX CALCIUM POLYCARBOPHIL PUBLIX SUPER MARKETS, INC 02e3f4ce-8961-425c-98a9-3b9d66709ca5 2025-10-28 Warnings Exact identifier application number: M007 Publix Women Laxative BISACODYL PUBLIX SUPER MARKETS, INC 03eeca55-f239-4a01-a900-c1943f27a834 2025-10-28 Warnings Exact identifier application number: M007 Publix Fiber Therapy Orange Smooth PSYLLIUM HUSK PUBLIX SUPER MARKETS, INC b9c54c20-cd82-4627-9217-a66834db4799 2025-10-28 Warnings Exact identifier application number: M007 Publix Fiber Therapy Sugar Free PSYLLIUM HUSK PUBLIX SUPER MARKETS, INC ed3dc80a-a243-4013-9886-b148e3e3b662 2025-10-28 Warnings Exact identifier application number: M007
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 17433-9877-2 17433987702 2 TUBE in 1 CONTAINER (17433-9877-2) / 5 mL in 1 TUBE (17433-9877-0) 2 tube 2024-01-26 No No Current