Dry Eye Relief
- Product NDC
- 53799-300
- 11-digit product format
- 537990300
- Labeler code
- 53799
- Product ID
- 53799-300_0e1c06e0-df5f-4a0c-894c-70f1517dc891
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Atropa Belladonna and Euphrasia Stricta and Mercuric Chloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Similasan AG
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-10-02
- Marketing end
- 0000-00-00
- Substance
- ATROPA BELLADONNA; EUPHRASIA STRICTA; MERCURIC CHLORIDE
- Active strength
- 6 [hp_X]/.4mL; [hp_X]/.4mL; [hp_X]/.4mL
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|
| 53799-300-12 | Dry Eye Relief | 0.4 mL in 1 VIAL, SINGLE-USE | SOLUTION/ DROPS | 0.4 | | 3 |
| 53799-300-12 | Dry Eye Relief | 20 in 1 CARTON | SOLUTION/ DROPS | 20 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53799-300 | DRY EYE RELIEF (ATROPA BELLADONNA AND EUPHRASIA STRICTA AND MERCURIC CHLORIDE) SOLUTION/ DROPS [SIMILASAN AG] | 3 | Legacy NDC, 2 package rows | 20230106_10962b03-2432-4efa-a020-d8edddd92763.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53799-300-12 | 53799030012 | 20 VIAL, SINGLE-USE in 1 CARTON (53799-300-12) > .4 mL in 1 VIAL, SINGLE-USE | 2020-10-02 | 0000-00-00 | No | No | Current |