ENEMEEZ Plus

Product NDC: 17433-9877
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

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1670ca59-7275-4ac6-bef4-674a7b24c7b3	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	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 Billing Units#

Package NDC, Billing unit, Product NDC table
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 table
Ingredient	Type	UNII	DailyMed label	SPL version
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

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 9 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stool Softener plus Stimulant Laxative	DOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MG	CARDINAL HEALTH, 110 DBA LEADER	3fd9ba76-42f8-4ebe-b1bc-f81f08e702ce	2026-03-06	Warnings	Exact identifier application number: M007
Magnesium Citrate	EQUATE MAGNESIUM CITRATE ORAL SOLUTION - LEMON	Walmart Inc.	484d0421-59ea-3783-e063-6394a90af633	2026-03-04	Warnings	Exact identifier application number: M007
Magnesium Citrate	EQUATE MAGNESIUM CITRATE ORAL SOLUTION - CHERRY	Walmart Inc.	484c2586-9e6f-1ce5-e063-6394a90a0d81	2026-03-04	Warnings	Exact identifier application number: M007
Magnesium Citrate	EQUATE MAGNESIUM CITRATE ORAL SOLUTION - GRAPE	Walmart Inc.	450ddcbd-7ccd-3670-e063-6294a90ac2bd	2026-03-04	Warnings	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Amazon.com Services LLC	787ec4b0-c6c5-44ab-a53d-d6d25304f95e	2026-03-03	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	Old East Main Co.	3d0d63d7-640d-4e54-a6fd-6b265c79be09	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	Old East Main Co.	9b3b6cea-ab83-4b7c-a425-fd0ac7df426c	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	Old East Main Co.	51ed515b-cc51-4ea1-b612-090476135005	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Old East Main Co.	a8af6e2d-0052-4fc9-a51a-c9dbeb1ad3f5	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	Chain Drug Marketing Association	629c5817-13b7-4527-8998-93131ee3529e	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	Chain Drug Marketing Association	4df97cdc-e7a2-4350-8f95-a679cdcaff64	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	Chain Drug Marketing Association	46b26b44-e065-4337-a071-fa036f897140	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	Chain Drug Marketing Association	ef163b24-ce92-4cbc-b45a-4fae3b511949	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Chain Drug Marketing Association	4ee26633-8eb1-4c68-a768-20460404533a	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M007
Mineral Oil	MINERAL OIL	Chain Drug Marketing Association	3bfdad9c-ac58-4e92-b952-555e8a8351cd	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	The Kroger Co.	2bcab227-42b6-4bff-8363-f6800665755b	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	The Kroger Co.	a87dceb2-da73-4d3a-b87c-db2af10471bf	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M007
Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	The Kroger Co.	3ae7e275-7bbc-4e62-b30f-013c40a89949	2026-02-27	Warnings	Exact identifier application number: M007
Sennosides	SENNOSIDES	CVS Pharmacy, Inc	0b7736df-c7de-7d00-e063-6294a90aa57e	2026-02-26	Warnings	Exact identifier application number: M007
DOCUSATE SODIUM	DOCUSATE SODIUM	PD-Rx Pharmaceuticals, Inc.	5d300ea7-78eb-4e19-8333-1e42c73c4c54	2026-02-26	Warnings	Exact identifier application number: M007

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
U3RSY48JW5	BENZOCAINE	94-09-7	BENZOCAINE
F05Q2T2JA0	DOCUSATE SODIUM	577-11-7	DOCUSATE SODIUM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1192984	docusate sodium 283 MG / benzocaine 20 MG in 5 mL Enema	PSN	1670ca59-7275-4ac6-bef4-674a7b24c7b3	22
1192986	Enemeez Plus 283 MG / 20 MG in 5 mL Enema	PSN	1670ca59-7275-4ac6-bef4-674a7b24c7b3	22
1192986	benzocaine 4 MG/ML / docusate sodium 56.6 MG/ML Enema [Enemeez Plus]	SBD	1670ca59-7275-4ac6-bef4-674a7b24c7b3	22
1192984	benzocaine 4 MG/ML / docusate sodium 56.6 MG/ML Enema	SCD	1670ca59-7275-4ac6-bef4-674a7b24c7b3	22
1192984	benzocaine 20 MG / docusate sodium 283 MG per 5 ML Enema	SY	1670ca59-7275-4ac6-bef4-674a7b24c7b3	22
1192984	Benzocaine 4 MG/ML / DOSS Sodium 56.6 MG/ML Enema	SY	1670ca59-7275-4ac6-bef4-674a7b24c7b3	22
1192986	Benzocaine 4 MG/ML / DOSS Sodium 56.6 MG/ML Enema [Enemeez Plus]	SY	1670ca59-7275-4ac6-bef4-674a7b24c7b3	22
1192986	Enemeez Plus (benzocaine 20 MG / docusate sodium 283 MG) per 5 ML Enema	SY	1670ca59-7275-4ac6-bef4-674a7b24c7b3	22

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
17433-9877-0	17433987700	5 mL in 1 TUBE	5 ml					Historical
17433-9877-1	17433987701	1 TUBE in 1 CONTAINER (17433-9877-1) / 5 mL in 1 TUBE (17433-9877-0)	1 tube	2025-05-27		Yes	No	Current
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
17433-9877-3	17433987703	30 TUBE in 1 CONTAINER (17433-9877-3) / 5 mL in 1 TUBE (17433-9877-0)	30 tube	2012-06-15	0000-00-00	No	No	Current
17433-9877-4	17433987704	65 TUBE in 1 CONTAINER (17433-9877-4) / 5 mL in 1 TUBE (17433-9877-0)	65 tube	2026-06-30		No	No	Current
17433-9877-5	17433987705	5 TUBE in 1 CONTAINER (17433-9877-5) / 5 mL in 1 TUBE (17433-9877-0)	5 tube	2022-01-14	0000-00-00	No	No	Current
17433-9877-6	17433987706	35 TUBE in 1 CONTAINER (17433-9877-6) / 5 mL in 1 TUBE (17433-9877-0)	35 tube	2021-10-08	0000-00-00	No	No	Current
17433-9877-7	17433987707	6 TUBE in 1 CONTAINER (17433-9877-7) / 5 mL in 1 TUBE (17433-9877-0)	6 tube	2025-07-15		No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Enemeez® Plus	Quest Products, LLC \| Enemeez LLC DBA Summit Pharmaceuticals	2026-06-30	HUMAN OTC DRUG LABEL	23