Scandium Oxydatum

Product NDC
37662-2990
Type
HUMAN OTC DRUG
Nonproprietary name
Scandium Oxydatum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Substance
SCANDIUM OXIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
37662-2990-1200 PELLET in 1 VIAL, GLASS (37662-2990-1) 2023-04-20NoHistorical
37662-2990-21200 PELLET in 1 BOTTLE, GLASS (37662-2990-2) 2023-04-20NoHistorical
37662-2990-34000 PELLET in 1 BOTTLE, GLASS (37662-2990-3) 2023-04-20NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Scandium Oxydatum - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2023-04-20HUMAN OTC DRUG LABEL1