warnings
Warnings For rectal use only. This is not a suppository. Do not take orally. Individuals with sensitivity to Benzocaine should not use this product.
ENEMEEZ Plus
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- ENEMEEZ Plus
- Generic name
- DOCUSATE SODIUM AND BENZOCAINE
- Manufacturer
- Quest Products, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1670ca59-7275-4ac6-bef4-674a7b24c7b3
- SPL ID
- 557c260c-c8fb-da2f-e063-6294a90a5501
- Version
- 23
- Effective date
- 2026-06-30
- Source export date
- 2026-10-30
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:59:46
| Harmonized routes |
|---|
| RECTAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M007 | openfda.application_number | |
| brand name | ENEMEEZ Plus | openfda.brand_name | |
| generic name | DOCUSATE SODIUM AND BENZOCAINE | openfda.generic_name | |
| manufacturer name | Quest Products, LLC | openfda.manufacturer_name | |
| ndc | package | 17433-9877-5 | openfda.package_ndc |
| ndc | package | 17433-9877-7 | openfda.package_ndc |
| ndc | package | 17433-9877-3 | openfda.package_ndc |
| ndc | package | 17433-9877-4 | openfda.package_ndc |
| ndc | package | 17433-9877-0 | openfda.package_ndc |
| ndc | package | 17433-9877-6 | openfda.package_ndc |
| ndc | package | 17433-9877-2 | openfda.package_ndc |
| ndc | package | 17433-9877-1 | openfda.package_ndc |
| ndc | product | 17433-9877 | openfda.product_ndc |
| ndc11 | package | 17433987701 | derived:openfda.package_ndc |
| ndc11 | package | 17433987704 | derived:openfda.package_ndc |
| ndc11 | package | 17433987702 | derived:openfda.package_ndc |
| ndc11 | package | 17433987705 | derived:openfda.package_ndc |
| ndc11 | package | 17433987700 | derived:openfda.package_ndc |
| ndc11 | package | 17433987706 | derived:openfda.package_ndc |
| ndc11 | package | 17433987703 | derived:openfda.package_ndc |
| ndc11 | package | 17433987707 | derived:openfda.package_ndc |
| rxcui | 1192984 | openfda.rxcui | |
| rxcui | 1192986 | openfda.rxcui | |
| spl id | 557c260c-c8fb-da2f-e063-6294a90a5501 | id | |
| spl set id | 1670ca59-7275-4ac6-bef4-674a7b24c7b3 | set_id | |
| unii | U3RSY48JW5 | openfda.unii | |
| unii | F05Q2T2JA0 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.