Urtica dioica ex herba Essence Special Order

Product NDC
48951-9189
11-digit product format
489519189
Labeler code
48951
Product ID
48951-9189_6b2ae27e-e843-d1b0-e053-2991aa0add64
Type
HUMAN OTC DRUG
Nonproprietary name
Urtica dioica ex herba Essence Special Order
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
URTICA DIOICA LEAF
Active strength
1 [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 productproduct48951-9189IInactivated by FDA2026-08-07
excluded packagepackage48951-918948951-9189-3IInactivated by FDA2026-08-07

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9189-3Urtica dioica ex herba Essence Special Order125 mL in 1 BOTTLE, GLASSLIQUID1252

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9189URTICA DIOICA EX HERBA ESSENCE SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20180502_6b96e235-ae65-4cb2-830e-24c0ec8b73a0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9189-348951918903125 mL in 1 BOTTLE, GLASS (48951-9189-3) 125 ml2009-09-010000-00-00NoNoCurrent