USTILAGO MAIDIS

Product NDC
0220-5153
11-digit product format
002205153
Labeler code
0220
Product ID
0220-5153_1e6649ad-2fa6-6737-e063-6394a90a7857
Type
HUMAN OTC DRUG
Nonproprietary name
USTILAGO MAYDIS
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
USTILAGO MAYDIS
Active strength
30 [hp_C]/30[hp_C]
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
USTILAGO MAIDIS
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
USTILAGO MAYDIS30 [hp_C]/30[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4K7Z7K7SWG

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-5153-412023-11-15C16284748780-1f386c64a-1646-0266-e053-dadaa90a7c1aUSTILAGO MAIDIS 30C
0220-5153-412023-01-30C16284748780-1f386c64a-1646-0266-e053-dadaa90a7c1aUSTILAGO MAIDIS 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-5153-41USTILAGO MAIDIS30 [hp_C] in 1 TUBEPELLET303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-5153USTILAGO MAIDIS (USTILAGO MAYDIS) PELLET [BOIRON]3Current NDC, Legacy NDC, 1 package rows20240730_861b3c1d-3b13-6ea6-e053-2991aa0ab4dc.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-5153-410022051534130 [hp_C] in 1 TUBE (0220-5153-41) 1983-03-030000-00-00NoNoCurrent