Mercurius vivus 8

Product NDC
48951-7044
11-digit product format
489517044
Labeler code
48951
Product ID
48951-7044_6d5d4380-05e1-504d-e053-2991aa0aa3b7
Type
HUMAN OTC DRUG
Nonproprietary name
Mercurius vivus 8
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
MERCURY
Active strength
8 [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
48951-7044-1Mercurius vivus 810 in 1 BOXLIQUID103
48951-7044-1Mercurius vivus 81 mL in 1 AMPULELIQUID13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MERCURYACTIVE INGREDIENTFXS1BY2PGLMERCURIUS VIVUS 8 LIQUID [URIEL PHARMACY INC.]1
MERCURYACTIVE MOIETYFXS1BY2PGLMERCURIUS VIVUS 8 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XMERCURIUS VIVUS 8 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RMERCURIUS VIVUS 8 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7044MERCURIUS VIVUS 8 LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 2 package rows20180529_571b14fe-ab7a-4b09-9ca8-1bb726048118.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-7044-14895170440110 AMPULE in 1 BOX (48951-7044-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent