BLATTA ORIENTALIS

Product NDC
0220-0865
11-digit product format
002200865
Labeler code
0220
Product ID
0220-0865_0c0490ee-23f3-1cdb-e063-6394a90a8185
Type
HUMAN OTC DRUG
Nonproprietary name
BLATTA ORIENTALIS
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-01-01
Substance
BLATTA ORIENTALIS
Active strength
200 [kp_C]/200[kp_C]
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Insect Proteins [CS], Non-Standardized Insect 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
BLATTA ORIENTALIS
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BLATTA ORIENTALIS200 [kp_C]/200[kp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii535787266D

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0865-41BLATTA ORIENTALIS200 [kp_C] in 1 TUBEPELLET2001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0865BLATTA ORIENTALIS PELLET [BOIRON]1Current NDC, 1 package rows20240101_0c0490ee-23f2-1cdb-e063-6394a90a8185.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
0220-0865-4100220086541200 [kp_C] in 1 TUBE (0220-0865-41) 2024-01-01NoNoHistorical