GoodSense Advanced Relief Eye
- Product NDC
- 50804-019
- 11-digit product format
- 508040019
- Labeler code
- 50804
- Product ID
- 50804-019_98fbd4b0-43b0-098b-e053-2a95a90a6645
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextran 70, Polyethylene glycol 400, Povidone, and Tetrahydrozoline HCI
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Geiss, Destin & Dunn, Inc.
- Application
- part349
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-03-24
- Marketing end
- 0000-00-00
- Substance
- DEXTRAN 70; POLYETHYLENE GLYCOL 400; POVIDONE; TETRAHYDROZOLINE HYDROCHLORIDE
- Active strength
- 1 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50804-019-05 | 50804001905 | 1 BOTTLE, DROPPER in 1 BOX (50804-019-05) > 15 mL in 1 BOTTLE, DROPPER | 2016-03-24 | 0000-00-00 | No | No | Current |