Rumex crispus

Product NDC
0220-4458
11-digit product format
002204458
Labeler code
0220
Product ID
0220-4458_f7073903-d494-3ff7-e053-6294a90a6902
Type
HUMAN OTC DRUG
Nonproprietary name
RUMEX CRISPUS ROOT
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
RUMEX CRISPUS ROOT
Active strength
200 [kp_C]/200[kp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
RUMEX CRISPUS ROOT200 [kp_C]/200[kp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9N1RM2S62C

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-4458-412023-03-16C16284748780-1f386c649-bdd1-0266-e053-dadaa90a7c1aRumex crispus 200CK
0220-4458-412023-01-30C16284748780-1f386c649-bdd1-0266-e053-dadaa90a7c1aRumex crispus 200CK

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-4458-41Rumex crispus200 [kp_C] in 1 TUBEPELLET2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-4458RUMEX CRISPUS (RUMEX CRISPUS ROOT ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230317_86bb1843-8c0b-515d-e053-2991aa0ae6cc.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-4458-4100220445841200 [kp_C] in 1 TUBE (0220-4458-41) 1983-03-030000-00-00NoNoCurrent