T-19

Product NDC
58264-0264
11-digit product format
582640264
Labeler code
58264
Product ID
58264-0264_2b539c7f-71ec-1665-e063-6294a90ab35a
Type
HUMAN OTC DRUG
Nonproprietary name
LARIX DECIDUA WHOLE
Dosage form
SOLUTION
Route
SUBLINGUAL
Labeler
DNA Labs, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1990-01-01
Substance
LARIX DECIDUA WHOLE
Active strength
30 [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
T-19
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LARIX DECIDUA WHOLE30 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO8554H2U9W

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0264-12020-01-31C16284748780-19d75b9cf-e699-f424-e053-dadaa90a57ceT-19

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0264-1T-1929.57 mL in 1 BOTTLE, GLASSSOLUTION29.576

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0264T-19 (LARIX DECIDUA WHOLE) SOLUTION [DNA LABS, INC.]6Current NDC, Legacy NDC, 1 package rows20250112_4dd99a36-ba4d-47d7-98a2-897aa2fdf4a3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58264-0264-15826402640129.57 mL in 1 BOTTLE, GLASS (58264-0264-1) 29.57 ml1990-01-010000-00-00NoNoCurrent