Glycyrrhiza Glabra

Product NDC
37662-0767
11-digit product format
376620767
Labeler code
37662
Product ID
37662-0767_e34062cf-5f3e-fcc5-e053-2995a90afc14
Type
HUMAN OTC DRUG
Nonproprietary name
Glycyrrhiza Glabra
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-07-07
Substance
GLYCYRRHIZA GLABRA
Active strength
200 [hp_C]/1
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
2788Z9758HGLYCYRRHIZA GLABRA84775-66-6GLYCYRRHIZA GLABRA

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-0767-137662076701200 PELLET in 1 VIAL, GLASS (37662-0767-1) 200 pellet2022-07-07NoNoHistorical
37662-0767-237662076702500 PELLET in 1 VIAL, GLASS (37662-0767-2) 500 pellet2022-07-07NoNoHistorical
37662-0767-3376620767033000 PELLET in 1 BOTTLE, GLASS (37662-0767-3) 3000 pellet2022-07-07NoNoHistorical
37662-0767-43766207670410000 PELLET in 1 BOTTLE, GLASS (37662-0767-4) 10000 pellet2022-07-07NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Glycyrrhiza Glabra - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2022-07-07HUMAN OTC DRUG LABEL1