FDA.reportPublic FDA data

Euphrasia 3X

Product NDC
48951-4156
11-digit product format
489514156
Labeler code
48951
Product ID
48951-4156_93ca023f-bbd0-cd38-e053-2a95a90a7d46
Type
HUMAN OTC DRUG
Nonproprietary name
Euphrasia 3X
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
EUPHRASIA STRICTA
Active strength
3 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-4156IInactivated by FDA2026-08-03
excluded packagepackage48951-415648951-4156-1IInactivated by FDA2026-08-03

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4156-1Euphrasia 3X1 in 1 BAGLIQUID12
48951-4156-1Euphrasia 3X10 mL in 1 BOTTLE, DROPPERLIQUID102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4156EUPHRASIA 3X LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 2 package rows20241010_93ca023f-bbcf-cd38-e053-2a95a90a7d46.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
48951-4156-1489514156011 BOTTLE, DROPPER in 1 BAG (48951-4156-1) > 10 mL in 1 BOTTLE, DROPPER2009-09-010000-00-00NoNoCurrent