FDA.reportPublic FDA data

Thuja e summ. 6X

Product NDC
48951-9361
11-digit product format
489519361
Labeler code
48951
Product ID
48951-9361_cf5aff6e-7abf-4de9-e053-2a95a90a6b1a
Type
HUMAN OTC DRUG
Nonproprietary name
Thuja e summ. 6X
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
THUJA OCCIDENTALIS WHOLE
Active strength
6 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2022-12-31
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 productproduct48951-9361IInactivated by FDA2026-08-11
excluded packagepackage48951-936148951-9361-3IInactivated by FDA2026-08-11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9361-3Thuja e summ. 6X60 mL in 1 BOTTLE, DROPPERLIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9361THUJA E SUMM. 6X LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20211028_c1ae6618-a65b-51e1-e053-2995a90af5fe.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9361-34895193610360 mL in 1 BOTTLE, DROPPER (48951-9361-3) 60 ml2009-09-010000-00-00NoNoCurrent