DocuSol Plus
- Product NDC
- 17433-9883
- 11-digit product format
- 174339883
- Labeler code
- 17433
- Product ID
- 17433-9883_ecfb3572-aff2-375f-e053-2995a90ad328
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- docusate sodium w/benzocaine
- Dosage form
- LIQUID
- Route
- RECTAL
- Labeler
- Enemeez LLC DBA Summit Pharmaceuticals
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-07-12
- Marketing end
- 2024-10-31
- Substance
- BENZOCAINE; DOCUSATE SODIUM
- Active strength
- 20 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17433-9883-5 | 17433988305 | 5 TUBE in 1 BOX (17433-9883-5) > 5 mL in 1 TUBE (17433-9883-1) | 5 tube | 2013-07-12 | 0000-00-00 | No | No | Current |