FDA.reportPublic FDA data

GLYCYRRHIZA GLABRA

Product NDC
0220-2305
11-digit product format
002202305
Labeler code
0220
Product ID
0220-2305_0a0d5748-6ceb-0f47-e063-6294a90a154e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
GLYCYRRHIZA GLABRA
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
GLYCYRRHIZA GLABRA
Active strength
30 [hp_C]/30[hp_C]
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

Additional Listing Data#

Finished product
Yes
Brand name base
GLYCYRRHIZA GLABRA
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GLYCYRRHIZA GLABRA30 [hp_C]/30[hp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2788Z9758HInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
7d7b46d9-b980-eaf0-e053-2a91aa0ae0f4Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-2305-412023-11-13C16284748780-1f386c64a-0ad7-0266-e053-dadaa90a7c1aGlycyrrhiza glabra 30C
0220-2305-412023-01-30C16284748780-1f386c64a-0ad7-0266-e053-dadaa90a7c1aGlycyrrhiza glabra 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-2305-41GLYCYRRHIZA GLABRA30 [hp_C] in 1 TUBEPELLET303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-2305GLYCYRRHIZA GLABRA PELLET [BOIRON]3Current NDC, Legacy NDC, 1 package rows20231114_7d7b46d9-b980-eaf0-e053-2a91aa0ae0f4.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GLYCYRRHIZA GLABRAGLYCYRRHIZA GLABRABoiron7d7b46d9-b980-eaf0-e053-2a91aa0ae0f42023-11-13Exact identifier
ndc (product): 0220-2305

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-2305-410022023054130 [hp_C] in 1 TUBE (0220-2305-41) 1983-03-030000-00-00NoNoCurrent