Chamomilla

Product NDC
76472-3012
11-digit product format
764723012
Labeler code
76472
Product ID
76472-3012_2ddc3214-553a-dc02-e063-6394a90a0464
Type
HUMAN OTC DRUG
Nonproprietary name
MATRICARIA RECUTITA
Dosage form
PELLET
Route
SUBLINGUAL
Labeler
SEVENE USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-11-24
Substance
MATRICARIA RECUTITA
Active strength
200 [kp_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
Chamomilla
Brand name suffix
200ck
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MATRICARIA RECUTITA200 [kp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG0R4UBI2ZZ

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-3012-1Chamomilla200ck80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-3012CHAMOMILLA 200CK (MATRICARIA RECUTITA) PELLET [SEVENE USA]4Current NDC, Legacy NDC, 1 package rows20250213_c8d5b230-9ef9-d1f4-e053-2995a90ac0e6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76472-3012-17647230120180 PELLET in 1 CYLINDER (76472-3012-1) 80 pellet2011-11-240000-00-00NoNoCurrent