Rhus Glabra

Product NDC
37662-1374
Type
HUMAN OTC DRUG
Nonproprietary name
Rhus Glabra
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Substance
RHUS GLABRA TOP
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
37662-1374-180 PELLET in 1 VIAL, GLASS (37662-1374-1) 2022-08-18NoHistorical
37662-1374-2200 PELLET in 1 VIAL, GLASS (37662-1374-2) 2022-08-18NoHistorical
37662-1374-31200 PELLET in 1 BOTTLE, GLASS (37662-1374-3) 2022-08-18NoHistorical
37662-1374-44000 PELLET in 1 BOTTLE, GLASS (37662-1374-4) 2022-08-18NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Rhus Glabra - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2022-08-18HUMAN OTC DRUG LABEL1