Gelsemium sempervirens

Product NDC
71919-312
11-digit product format
719190312
Labeler code
71919
Product ID
71919-312_7e4f146c-b3b7-cd7c-e053-2991aa0a3658
Type
HUMAN OTC DRUG
Nonproprietary name
GELSEMIUM SEMPERVIRENS ROOT
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2010-02-03
Marketing end
0000-00-00
Substance
GELSEMIUM SEMPERVIRENS ROOT
Active strength
30 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#