Ustilago maidis

Product NDC
0220-5154
11-digit product format
002205154
Labeler code
0220
Product ID
0220-5154_1e662cb0-4ce9-c873-e063-6294a90af16b
Type
HUMAN OTC DRUG
Nonproprietary name
USTILAGO MAYDIS
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-07-29
Substance
USTILAGO MAYDIS
Active strength
200 [kp_C]/200[kp_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 MAYDIS200 [kp_C]/200[kp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4K7Z7K7SWG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-5154-41Ustilago maidis200 [kp_C] in 1 TUBEPELLET2001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-5154USTILAGO MAIDIS (USTILAGO MAYDIS) PELLET [BOIRON]1Current NDC, 1 package rows20240730_1e662cb0-4ce8-c873-e063-6294a90af16b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
0220-5154-4100220515441200 [kp_C] in 1 TUBE (0220-5154-41) 2024-07-29NoNoHistorical