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 29 of 41 · 817 matching rows.
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