Aurum 30

Product NDC
48951-1178
11-digit product format
489511178
Labeler code
48951
Product ID
48951-1178_6c68afb4-66b7-0b60-e053-2991aa0acbdc
Type
HUMAN OTC DRUG
Nonproprietary name
Aurum 30
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
30 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-1178-12026-01-29C16284748780-149896155-ae2b-586f-e063-e6dba90add90Aurum 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1178-1Aurum 301 mL in 1 AMPULELIQUID15
48951-1178-1Aurum 3010 in 1 BOXLIQUID105

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GOLDACTIVE INGREDIENT79Y1949PYOAURUM 30 LIQUID [URIEL PHARMACY INC.]1
GOLDACTIVE MOIETY79Y1949PYOAURUM 30 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XAURUM 30 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RAURUM 30 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1178AURUM 30 LIQUID [URIEL PHARMACY INC.]5Legacy NDC, 2 package rows20240116_d3280b85-a9d4-4858-8546-5418364e79d4.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1178-14895111780110 AMPULE in 1 BOX (48951-1178-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent