Helleborus comp. C

Product NDC
48951-5119
11-digit product format
489515119
Labeler code
48951
Product ID
48951-5119_8f77df41-58c0-8267-e053-2995a90a90e2
Type
HUMAN OTC DRUG
Nonproprietary name
Helleborus comp. C
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
SILVER; LEAD; CHELIDONIUM MAJUS; FORMICA RUFA; BOS TAURUS SPLEEN; HELLEBORUS NIGER ROOT; ANTIMONY
Active strength
20 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-5119-1Helleborus comp. C10 in 1 BOXLIQUID103
48951-5119-1Helleborus comp. C1 mL in 1 AMPULELIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-5119HELLEBORUS COMP. C LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 2 package rows20241219_8f77df41-58bf-8267-e053-2995a90a90e2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-5119-14895151190110 AMPULE in 1 BOX (48951-5119-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent