Helleborus comp. E

Product NDC
48951-5120
11-digit product format
489515120
Labeler code
48951
Product ID
48951-5120_902ac093-cfb3-277f-e053-2995a90a8348
Type
HUMAN OTC DRUG
Nonproprietary name
Helleborus comp. E
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
CHINESE YAM; HELLEBORUS NIGER ROOT; LEAD; KALANCHOE DAIGREMONTIANA LEAF; ROSMARINUS OFFICINALIS FLOWERING TOP; ANTIMONY; GOLD; HELLEBORUS FOETIDUS ROOT
Active strength
3 [hp_X]/mL; [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
48951-5120-3Helleborus comp. E60 mL in 1 BOTTLE, DROPPERLIQUID603

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-5120HELLEBORUS COMP. E LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 1 package rows20241219_902ac093-cfb2-277f-e053-2995a90a8348.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-5120-34895151200360 mL in 1 BOTTLE, DROPPER (48951-5120-3) 60 ml2009-09-010000-00-00NoNoCurrent