FDA.reportPublic FDA data

Echinacea Angustifolia

Product NDC
37662-0665
11-digit product format
376620665
Labeler code
37662
Product ID
37662-0665_e1fa828f-be29-0fa0-e053-2a95a90a2f91
Type
HUMAN OTC DRUG
Nonproprietary name
Echinacea Angustifolia
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-06-21
Substance
ECHINACEA ANGUSTIFOLIA WHOLE
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
Echinacea Angustifolia
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ECHINACEA ANGUSTIFOLIA WHOLE6 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiVB06AV5US8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-0665-1Echinacea Angustifolia200 in 1 VIAL, GLASSPELLET2001
37662-0665-2Echinacea Angustifolia1200 in 1 BOTTLE, GLASSPELLET12001
37662-0665-3Echinacea Angustifolia4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-0665ECHINACEA ANGUSTIFOLIA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20220623_e1fa828f-be28-0fa0-e053-2a95a90a2f91.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-0665-137662066501200 PELLET in 1 VIAL, GLASS (37662-0665-1) 200 pellet2022-06-210000-00-00NoNoCurrent
37662-0665-2376620665021200 PELLET in 1 BOTTLE, GLASS (37662-0665-2) 1200 pellet2022-06-210000-00-00NoNoCurrent
37662-0665-3376620665034000 PELLET in 1 BOTTLE, GLASS (37662-0665-3) 4000 pellet2022-06-210000-00-00NoNoCurrent