Gelsemium sempervirens

Product NDC
0220-2255
11-digit product format
002202255
Labeler code
0220
Product ID
0220-2255_41ede67a-9e2c-bbfd-e063-6294a90aff19
Type
HUMAN OTC DRUG
Nonproprietary name
GELSEMIUM SEMPERVIRENS ROOT
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
GELSEMIUM SEMPERVIRENS ROOT
Active strength
1 [hp_M]/[hp_M]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GELSEMIUM SEMPERVIRENS ROOT1 [hp_M]/[hp_M]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii639KR60Q1Q

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-2255-41Gelsemium sempervirens1 [hp_M] in 1 TUBEPELLET13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-2255GELSEMIUM SEMPERVIRENS (GELSEMIUM SEMPERVIRENS ROOT ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231222_85a29d28-b47b-e877-e053-2991aa0ac049.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-2255-41002202255411 [hp_M] in 1 TUBE (0220-2255-41) 1983-03-030000-00-00NoNoCurrent