FDA.reportPublic FDA data

Rumex Crispus

Product NDC
37662-2001
11-digit product format
376622001
Labeler code
37662
Product ID
37662-2001_ee1ad771-9548-4272-e053-2a95a90aacc4
Type
HUMAN OTC DRUG
Nonproprietary name
Rumex Crispus
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-11-22
Substance
RUMEX CRISPUS ROOT
Active strength
6 [hp_C]/1
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 ROOT6 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9N1RM2S62C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2001-1Rumex Crispus200 in 1 VIAL, GLASSPELLET2001
37662-2001-2Rumex Crispus1200 in 1 BOTTLE, GLASSPELLET12001
37662-2001-3Rumex Crispus4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2001RUMEX CRISPUS PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20221124_ee1ad771-9547-4272-e053-2a95a90aacc4.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-2001-137662200101200 PELLET in 1 VIAL, GLASS (37662-2001-1) 200 pellet2022-11-220000-00-00NoNoCurrent
37662-2001-2376622001021200 PELLET in 1 BOTTLE, GLASS (37662-2001-2) 1200 pellet2022-11-220000-00-00NoNoCurrent
37662-2001-3376622001034000 PELLET in 1 BOTTLE, GLASS (37662-2001-3) 4000 pellet2022-11-220000-00-00NoNoCurrent