Rhus Glabra

Product NDC
37662-1378
11-digit product format
376621378
Labeler code
37662
Product ID
37662-1378_e68d0227-13a9-c6be-e053-2a95a90aacbd
Type
HUMAN OTC DRUG
Nonproprietary name
Rhus Glabra
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-08-18
Substance
RHUS GLABRA TOP
Active strength
1 [hp_M]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termMatched term
RHH784E0K6RHUS GLABRA TOPRHUS GLABRA TOP

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-1378-137662137801200 PELLET in 1 VIAL, GLASS (37662-1378-1) 200 pellet2022-08-18NoNoHistorical
37662-1378-237662137802500 PELLET in 1 VIAL, GLASS (37662-1378-2) 500 pellet2022-08-18NoNoHistorical
37662-1378-3376621378033000 PELLET in 1 BOTTLE, GLASS (37662-1378-3) 3000 pellet2022-08-18NoNoHistorical
37662-1378-43766213780410000 PELLET in 1 BOTTLE, GLASS (37662-1378-4) 10000 pellet2022-08-18NoNoHistorical

Related DailyMed Labels

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