BOBA HOMO

Product NDC
43742-1716
11-digit product format
437421716
Labeler code
43742
Product ID
43742-1716_f295efbe-3601-4453-b423-bd493d11ade7
Type
HUMAN OTC DRUG
Nonproprietary name
Babesia Microti, Borrelia Burgdorferi Nosode
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-10-07
Substance
BABESIA MICROTI; BORRELIA BURGDORFERI
Active strength
15; 15 [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
BOBA HOMO
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BABESIA MICROTI15 [hp_X]/mL
BORRELIA BURGDORFERI15 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1948X6KEG3, 0J8NV9V5Q8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-1716-1BOBA HOMO30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1716BOBA HOMO (BABESIA MICROTI, BORRELIA BURGDORFERI NOSODE) LIQUID [DESERET BIOLOGICALS, INC.]4Current NDC, Legacy NDC, 1 package rows20240221_dae13222-a407-4982-8caf-17397a815806.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-1716-14374217160130 mL in 1 BOTTLE, DROPPER (43742-1716-1) 30 ml2020-10-070000-00-00NoNoCurrent