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 UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4K7Z7K7SWGInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
861b3c1d-3b13-6ea6-e053-2991aa0ab4dcAvailable on FDA.report

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

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
USTILAGO MAIDISUSTILAGO MAYDISBoiron861b3c1d-3b13-6ea6-e053-2991aa0ab4dc2024-07-29Exact identifier
ndc (product): 0220-5153

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