Mercurius cyanatus 8

Product NDC
48951-7142
11-digit product format
489517142
Labeler code
48951
Product ID
48951-7142_55dacc7e-15c9-42a4-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Mercurius cyanatus 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
MERCURIC CYANIDE
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
48951-7142-1Mercurius cyanatus 810 in 1 BOXLIQUID102
48951-7142-1Mercurius cyanatus 81 mL in 1 AMPULELIQUID12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MERCURIC CYANIDEACTIVE INGREDIENTRWG7BD1032MERCURIUS CYANATUS 8 LIQUID [URIEL PHARMACY INC.]1
MERCURIC CYANIDEACTIVE MOIETYRWG7BD1032MERCURIUS CYANATUS 8 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XMERCURIUS CYANATUS 8 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RMERCURIUS CYANATUS 8 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7142MERCURIUS CYANATUS 8 LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 2 package rows20180530_b76db565-adc4-487f-b1b4-2947cfc6c21a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-7142-14895171420110 AMPULE in 1 BOX (48951-7142-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent