Drosera

Product NDC
53645-2001
11-digit product format
536452001
Labeler code
53645
Product ID
53645-2001_fe921a82-8032-f0fd-e053-6394a90af4af
Type
HUMAN OTC DRUG
Nonproprietary name
Drosera
Dosage form
LIQUID
Route
ORAL
Labeler
True Botanica, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-06-20
Substance
DROSERA INTERMEDIA
Active strength
6 [hp_X]/55mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DROSERA INTERMEDIA6 [hp_X]/55mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiB3G4A96QLY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53645-2001-3Drosera55 mL in 1 BOTTLELIQUID551

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53645-2001DROSERA LIQUID [TRUE BOTANICA, LLC]1Current NDC, 1 package rows20230710_fe91eee6-e240-64b7-e053-6394a90a4cf6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
53645-2001-35364520010355 mL in 1 BOTTLE (53645-2001-3) 55 ml2023-06-20NoNoCurrent