Gelsemium sempervirens

Product NDC
0220-2251
11-digit product format
002202251
Labeler code
0220
Product ID
0220-2251_41edab02-2c85-521b-e063-6294a90a365e
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
12 [hp_C]/12[hp_C]
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 ROOT12 [hp_C]/12[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii639KR60Q1Q

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-2251-41Gelsemium sempervirens12 [hp_C] in 1 TUBEPELLET123

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-2251GELSEMIUM SEMPERVIRENS (GELSEMIUM SEMPERVIRENS ROOT ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231222_85a29037-8c13-25e2-e053-2a91aa0a0845.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-2251-410022022514112 [hp_C] in 1 TUBE (0220-2251-41) 1983-03-030000-00-00NoNoCurrent