Dry Eye Relief Trial Size 15x

Product NDC
59262-376
11-digit product format
592620376
Labeler code
59262
Product ID
59262-376_57bc88f1-8161-4dae-a023-069eebe7083f
Type
HUMAN OTC DRUG
Nonproprietary name
Belladonna, Euphrasia officinalis, Mercurius sublimatus,
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Similasan Corporation
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2021-07-08
Marketing end
0000-00-00
Substance
ATROPA BELLADONNA; EUPHRASIA STRICTA; MERCURIC CHLORIDE
Active strength
6 [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL
NDC exclude flag
No
Listing certified through
2024-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59262-376-132025-01-30C16284748780-12cef2736-9109-d83d-e063-dadaa90ab31fDry Eye Relief Trial Size 15x

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59262-376-13Dry Eye Relief Trial Size 15x.4 mL in 1 VIAL, SINGLE-USESOLUTION/ DROPS.42

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59262-376DRY EYE RELIEF TRIAL SIZE 15X (BELLADONNA, EUPHRASIA OFFICINALIS, MERCURIUS SUBLIMATUS,) SOLUTION/ DROPS [SIMILASAN CORPORATION]2Legacy NDC, 1 package rows20230106_731a668e-facc-4be6-95d5-eb2907005312.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
59262-376-1359262037613.4 mL in 1 VIAL, SINGLE-USE (59262-376-13) 2021-07-080000-00-00NoNoCurrent