Thuja

Product NDC
59469-157
11-digit product format
594690157
Labeler code
59469
Product ID
59469-157_f076c9c6-31a0-4dff-b7cc-66e08f5ab00e
Type
HUMAN OTC DRUG
Nonproprietary name
Thuja occidentalis leafy twig
Dosage form
LIQUID
Route
ORAL
Labeler
PEKANA Naturheilmittel GmbH
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2005-05-01
Substance
THUJA OCCIDENTALIS LEAFY TWIG
Active strength
3 [hp_X]/50mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
THUJA OCCIDENTALIS LEAFY TWIG3 [hp_X]/50mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1NT28V9397

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59469-157-10Thuja1 in 1 BOXLIQUID16
59469-157-10Thuja50 mL in 1 BOTTLE, GLASSLIQUID506

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59469-157THUJA (THUJA OCCIDENTALIS LEAFY TWIG) LIQUID [PEKANA NATURHEILMITTEL GMBH]6Current NDC, Legacy NDC, 2 package rows20221224_f5538c6c-9d00-44cb-a097-25d2b027aa9c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
59469-157-10594690157101 BOTTLE, GLASS in 1 BOX (59469-157-10) / 50 mL in 1 BOTTLE, GLASS2005-05-010000-00-00NoNoCurrent