Aurum 20

Product NDC
48951-1177
11-digit product format
489511177
Labeler code
48951
Product ID
48951-1177_6b502268-3e81-7fcb-e053-2991aa0aabdc
Type
HUMAN OTC DRUG
Nonproprietary name
Aurum 20
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
GOLD
Active strength
20 [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
48951-1177-1Aurum 2010 in 1 BOXLIQUID103
48951-1177-1Aurum 201 mL in 1 AMPULELIQUID13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GOLDACTIVE INGREDIENT79Y1949PYOAURUM 20 LIQUID [URIEL PHARMACY INC.]1
GOLDACTIVE MOIETY79Y1949PYOAURUM 20 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XAURUM 20 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RAURUM 20 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1177AURUM 20 LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 2 package rows20180503_316ab962-a5d1-4591-9ef2-e97d281e7697.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1177-14895111770110 AMPULE in 1 BOX (48951-1177-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent