Bryonia

Product NDC
55714-9019
11-digit product format
557149019
Labeler code
55714
Product ID
55714-9019_e20b4111-4c6c-18c4-e053-2995a90a5e22
Type
HUMAN OTC DRUG
Nonproprietary name
Bryonia
Dosage form
LIQUID
Route
ORAL
Labeler
Newton Laboratories, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-06-22
Substance
BRYONIA ALBA ROOT
Active strength
10 [hp_X]/L
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BRYONIA ALBA ROOT10 [hp_X]/L

Harmonized Identifiers#

Field, Values table
FieldValues
UniiT7J046YI2B

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55714-9019-6Bryonia3 L in 1 JUGLIQUID31

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55714-9019BRYONIA LIQUID [NEWTON LABORATORIES, INC.]1Current NDC, Legacy NDC, 1 package rows20220626_e20b392e-37de-1c83-e053-2995a90a760b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55714-9019-6557149019063 L in 1 JUG (55714-9019-6) 3 l2022-06-220000-00-00NoNoCurrent