FDA.reportPublic FDA data

Anti Fungal

Product NDC
66096-143
11-digit product format
660960143
Labeler code
66096
Product ID
66096-143_d44bf70c-0a67-0c03-e053-2a95a90a6b53
Type
HUMAN OTC DRUG
Nonproprietary name
Baptisia Tinctoria, Calendula Officinalis, Thuja Occidentalis.
Dosage form
LIQUID
Route
ORAL
Labeler
OHM PHARMA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2016-02-10
Substance
BAPTISIA TINCTORIA ROOT; CALENDULA OFFICINALIS FLOWERING TOP; THUJA OCCIDENTALIS LEAFY TWIG
Active strength
1; 1; 1 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Anti Fungal
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BAPTISIA TINCTORIA ROOT1 [hp_X]/30mL
CALENDULA OFFICINALIS FLOWERING TOP1 [hp_X]/30mL
THUJA OCCIDENTALIS LEAFY TWIG1 [hp_X]/30mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5EF0HWI5WU, 18E7415PXQ, 1NT28V9397

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66096-143-02Anti Fungal30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66096-143ANTI FUNGAL (BAPTISIA TINCTORIA, CALENDULA OFFICINALIS, THUJA OCCIDENTALIS.) LIQUID [OHM PHARMA INC.]4Current NDC, Legacy NDC, 1 package rows20211230_ee3112c9-3af1-4d0f-ba22-f9bbcc5fe46d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66096-143-026609601430230 mL in 1 BOTTLE, DROPPER (66096-143-02) 30 ml2016-02-100000-00-00NoNoCurrent