Mercurius solubilis 12 Special Order

Product NDC
48951-7123
11-digit product format
489517123
Labeler code
48951
Product ID
48951-7123_55dae099-0014-4b76-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Mercurius solubilis 12 Special Order
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
MERCURIUS SOLUBILIS
Active strength
12 [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
48951-7123-1Mercurius solubilis 12 Special Order1 mL in 1 AMPULELIQUID12
48951-7123-1Mercurius solubilis 12 Special Order10 in 1 BOXLIQUID102

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MERCURIUS SOLUBILISACTIVE INGREDIENT324Y4038G2MERCURIUS SOLUBILIS 12 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
MERCURIUS SOLUBILISACTIVE MOIETY324Y4038G2MERCURIUS SOLUBILIS 12 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XMERCURIUS SOLUBILIS 12 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RMERCURIUS SOLUBILIS 12 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7123MERCURIUS SOLUBILIS 12 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 2 package rows20180529_79e4c101-3648-4679-b5a7-137753858da4.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-7123-14895171230110 AMPULE in 1 BOX (48951-7123-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent