Mandragora 5% Special Order

Product NDC
48951-7128
11-digit product format
489517128
Labeler code
48951
Product ID
48951-7128_15c22c9e-200c-4c3c-afd3-3a1743e5d867
Type
HUMAN OTC DRUG
Nonproprietary name
Mandragora 5% Special Order
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
MANDRAGORA OFFICINARUM ROOT
Active strength
1 [hp_X]/g
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-7128-52020-01-31C16284748780-19d75b9d1-1560-f424-e053-dadaa90a57ceMandragora 5% Special Order

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-7128-5Mandragora 5% Special Order60 g in 1 TUBEOINTMENT601

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7128MANDRAGORA 5% SPECIAL ORDER OINTMENT [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20141105_176814bd-b577-4d6e-83c6-f0539f0f4965.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
48951-7128-54895171280560 g in 1 TUBE60 gHistorical