Urtica Conchae

Product NDC
48951-9027
Requested package NDC
48951-9027-2
11-digit product format
489519027
Labeler code
48951
Product ID
48951-9027_6e10cc1b-1e7f-457d-e053-2a91aa0a1db3
Type
HUMAN OTC DRUG
Nonproprietary name
Urtica Conchae
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
OSTREA EDULIS SHELL; URTICA URENS; TIN
Active strength
2 [hp_X]/1; [hp_X]/1; [hp_X]/1
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage48951-902748951-9027-2IInactivated by FDA2026-10-16

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9027-2Urtica Conchae1350 in 1 BOTTLE, GLASSPELLET13504

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9027URTICA CONCHAE PELLET [URIEL PHARMACY INC.]4Legacy NDC, 1 package rows20241127_9fac8432-0a5a-4a90-8491-9e5d88e36d49.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9027-2489519027021350 PELLET in 1 BOTTLE, GLASS (48951-9027-2) 1350 pellet2009-09-010000-00-00NoNoCurrent