FDA.reportPublic FDA data

Aconitum Bryonia

Product NDC
48951-9170
11-digit product format
489519170
Labeler code
48951
Product ID
48951-9170_69803f70-5821-5af6-e053-2991aa0a9763
Type
HUMAN OTC DRUG
Nonproprietary name
Aconitum Bryonia
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
ACONITUM NAPELLUS; BRYONIA ALBA ROOT
Active strength
3 [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-9170IInactivated by FDA2026-10-21
excluded packagepackage48951-917048951-9170-3IInactivated by FDA2026-10-21

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9170-3Aconitum Bryonia10 in 1 BOXLIQUID104
48951-9170-3Aconitum Bryonia1 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACONITUM NAPELLUSACTIVE INGREDIENTU0NQ8555JDACONITUM BRYONIA LIQUID [URIEL PHARMACY INC.]1
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2BACONITUM BRYONIA LIQUID [URIEL PHARMACY INC.]1
ACONITUM NAPELLUSACTIVE MOIETYU0NQ8555JDACONITUM BRYONIA LIQUID [URIEL PHARMACY INC.]1
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2BACONITUM BRYONIA LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XACONITUM BRYONIA LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RACONITUM BRYONIA LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9170ACONITUM BRYONIA LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 2 package rows20180410_649c8c60-eb42-46c6-9a54-af80fdece66e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9170-34895191700310 AMPULE in 1 BOX (48951-9170-3) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent