Bryonia Stannum

Product NDC
48951-2086
11-digit product format
489512086
Labeler code
48951
Product ID
48951-2086_6c7d9173-6897-3d99-e053-2a91aa0a9a3d
Type
HUMAN OTC DRUG
Nonproprietary name
Bryonia Stannum
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
BRYONIA ALBA ROOT; TIN
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2086-1Bryonia Stannum10 in 1 BOXLIQUID105
48951-2086-1Bryonia Stannum1 mL in 1 AMPULELIQUID15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2BBRYONIA STANNUM LIQUID [URIEL PHARMACY INC.]1
TINACTIVE INGREDIENT387GMG9FH5BRYONIA STANNUM LIQUID [URIEL PHARMACY INC.]1
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2BBRYONIA STANNUM LIQUID [URIEL PHARMACY INC.]1
TINACTIVE MOIETY387GMG9FH5BRYONIA STANNUM LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XBRYONIA STANNUM LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RBRYONIA STANNUM LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2086BRYONIA STANNUM LIQUID [URIEL PHARMACY INC.]5Legacy NDC, 2 package rows20241219_e2a5de3e-526c-4a4b-9885-33c45d6f883a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-2086-14895120860110 AMPULE in 1 BOX (48951-2086-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent