T-2

Product NDC
58264-0247
11-digit product format
582640247
Labeler code
58264
Product ID
58264-0247_2b539a4e-f4be-fd07-e063-6294a90a32b9
Type
HUMAN OTC DRUG
Nonproprietary name
POPULUS TREMULOIDES WHOLE
Dosage form
SOLUTION
Route
SUBLINGUAL
Labeler
DNA Labs, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1990-01-01
Substance
POPULUS TREMULOIDES 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-2
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
POPULUS TREMULOIDES WHOLE30 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiMUN0TBE4PE

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0247-12022-04-27C16284748780-19d75b9d0-6967-f424-e053-dadaa90a57ceT-2
58264-0247-12020-01-31C16284748780-19d75b9d0-6967-f424-e053-dadaa90a57ceT-2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0247-1T-229.57 mL in 1 BOTTLE, GLASSSOLUTION29.574

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0247T-2 (POPULUS TREMULOIDES WHOLE) SOLUTION [DNA LABS, INC.]4Current NDC, Legacy NDC, 1 package rows20250112_0bc641a4-b8c7-4fae-b8d2-ebd25423c88f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58264-0247-15826402470129.57 mL in 1 BOTTLE, GLASS (58264-0247-1) 29.57 ml1990-01-010000-00-00NoNoCurrent