Thuja occidentalis

Product NDC
0220-5018
11-digit product format
002205018
Labeler code
0220
Product ID
0220-5018_445d93d7-efb3-ea8d-e063-6294a90ab98f
Type
HUMAN OTC DRUG
Nonproprietary name
THUJA OCCIDENTALIS LEAFY TWIG
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
THUJA OCCIDENTALIS LEAFY TWIG
Active strength
200 [kp_C]/200[kp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Thuja occidentalis
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
THUJA OCCIDENTALIS LEAFY TWIG200 [kp_C]/200[kp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1NT28V9397

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-5018-41Thuja occidentalis200 [kp_C] in 1 TUBEPELLET2003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-5018THUJA OCCIDENTALIS (THUJA OCCIDENTALIS LEAFY TWIG ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230124_8634de33-d56c-2bb1-e053-2a91aa0ae42f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-5018-4100220501841200 [kp_C] in 1 TUBE (0220-5018-41) 1983-03-030000-00-00NoNoCurrent