FDA.reportPublic FDA data

Bryophyllum Argentum

Product NDC
48951-2088
11-digit product format
489512088
Labeler code
48951
Product ID
48951-2088_6cb86761-361e-37a3-e053-2991aa0a05ef
Type
HUMAN OTC DRUG
Nonproprietary name
Bryophyllum Argentum
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
KALANCHOE DAIGREMONTIANA LEAF; SILVER; BOS TAURUS UTERUS
Active strength
3 [hp_X]/mL; [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 productproduct48951-2088DDiscontinued by firm2026-10-05
excluded packagepackage48951-208848951-2088-1DDiscontinued by firm2026-10-05

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
48951-2088-1Bryophyllum Argentum10 in 1 BOXLIQUID104
48951-2088-1Bryophyllum Argentum1 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BOS TAURUS UTERUSACTIVE INGREDIENT9169LW451GBRYOPHYLLUM ARGENTUM LIQUID [URIEL PHARMACY INC.]1
KALANCHOE DAIGREMONTIANA LEAFACTIVE INGREDIENTL6X13JKL8OBRYOPHYLLUM ARGENTUM LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE INGREDIENT3M4G523W1GBRYOPHYLLUM ARGENTUM LIQUID [URIEL PHARMACY INC.]1
BOS TAURUS UTERUSACTIVE MOIETY9169LW451GBRYOPHYLLUM ARGENTUM LIQUID [URIEL PHARMACY INC.]1
KALANCHOE DAIGREMONTIANA LEAFACTIVE MOIETYL6X13JKL8OBRYOPHYLLUM ARGENTUM LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE MOIETY3M4G523W1GBRYOPHYLLUM ARGENTUM LIQUID [URIEL PHARMACY INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GBRYOPHYLLUM ARGENTUM LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XBRYOPHYLLUM ARGENTUM LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RBRYOPHYLLUM ARGENTUM LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2088BRYOPHYLLUM ARGENTUM LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 2 package rows20240119_3beb6312-2117-4790-a517-4893f647e815.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-2088-14895120880110 AMPULE in 1 BOX (48951-2088-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent