FDA.reportPublic FDA data

Rhus Glabra

Product NDC
37662-1372
11-digit product format
376621372
Labeler code
37662
Product ID
37662-1372_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
6 [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Rhus Glabra
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
RHUS GLABRA TOP6 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiRHH784E0K6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-1372-1Rhus Glabra200 in 1 VIAL, GLASSPELLET2001
37662-1372-2Rhus Glabra1200 in 1 BOTTLE, GLASSPELLET12001
37662-1372-3Rhus Glabra4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-1372RHUS GLABRA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20220820_e68d0227-13a8-c6be-e053-2a95a90aacbd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-1372-137662137201200 PELLET in 1 VIAL, GLASS (37662-1372-1) 200 pellet2022-08-180000-00-00NoNoCurrent
37662-1372-2376621372021200 PELLET in 1 BOTTLE, GLASS (37662-1372-2) 1200 pellet2022-08-180000-00-00NoNoCurrent
37662-1372-3376621372034000 PELLET in 1 BOTTLE, GLASS (37662-1372-3) 4000 pellet2022-08-180000-00-00NoNoCurrent