FDA.reportPublic FDA data

Lycopodium clavatum

Product NDC
71919-429
11-digit product format
719190429
Labeler code
71919
Product ID
71919-429_7e56880c-50c2-e2c1-e053-2a91aa0ab6ef
Type
HUMAN OTC DRUG
Nonproprietary name
LYCOPODIUM CLAVATUM SPORE
Dosage form
LIQUID
Route
ORAL
Labeler
Washington Homeopathic Products
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2012-04-04
Marketing end
0000-00-00
Substance
LYCOPODIUM CLAVATUM SPORE
Active strength
30 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 5 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71919-429DDiscontinued by firm2026-07-31
excluded packagepackage71919-42971919-429-07DDiscontinued by firm2026-07-31
excluded packagepackage71919-42971919-429-08DDiscontinued by firm2026-07-31
excluded packagepackage71919-42971919-429-09DDiscontinued by firm2026-07-31
excluded packagepackage71919-42971919-429-10DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71919-429-077191904290715 mL in 1 VIAL, GLASS (71919-429-07) 15 ml2012-04-040000-00-00NoNoCurrent
71919-429-087191904290830 mL in 1 VIAL, GLASS (71919-429-08) 30 ml2012-04-040000-00-00NoNoCurrent
71919-429-097191904290950 mL in 1 BOTTLE, GLASS (71919-429-09) 50 ml2012-04-040000-00-00NoNoCurrent
71919-429-1071919042910100 mL in 1 BOTTLE, GLASS (71919-429-10) 100 ml2012-04-040000-00-00NoNoCurrent