GoodSense Irritation Relief Eye
- Product NDC
- 50804-018
- 11-digit product format
- 508040018
- Labeler code
- 50804
- Product ID
- 50804-018_8a9d6836-786e-49a6-834c-9f381ea31619
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tetrahydrozoline HCI, and Zinc sulfate
- 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
- TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE
- Active strength
- 0 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50804-018-05 | GoodSense Irritation Relief Eye | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | | 1 |
| 50804-018-05 | GoodSense Irritation Relief Eye | 1 in 1 BOX | SOLUTION/ DROPS | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50804-018 | GOODSENSE IRRITATION RELIEF EYE (TETRAHYDROZOLINE HCI, AND ZINC SULFATE) SOLUTION/ DROPS [GEISS, DESTIN & DUNN, INC.] | 1 | Legacy NDC, 2 package rows | 20160325_07ae9ea8-a25d-47b6-87ed-ae9364070d71.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 50804-018-05 | 50804001805 | 15 mL in 1 BOTTLE, DROPPER | 15 ml | Historical |