Aurum 21X

Product NDC
48951-1318
11-digit product format
489511318
Labeler code
48951
Product ID
48951-1318_48889afd-554b-a47f-e063-6394a90a9bb0
Type
HUMAN OTC DRUG
Nonproprietary name
Aurum 21X
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
GOLD
Active strength
21 [hp_X]/mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Aurum 21X
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GOLD21 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
79Y1949PYOInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
93f243c0-b963-9ea0-e053-2995a90aa852Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1318-1Aurum 21X10 in 1 BOXLIQUID103
48951-1318-1Aurum 21X1 mL in 1 AMPULELIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1318AURUM 21X LIQUID [URIEL PHARMACY INC.]2Current NDC, Legacy NDC, 2 package rows20250109_93f243c0-b963-9ea0-e053-2995a90aa852.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Aurum 21XAURUM 21XUriel Pharmacy Inc.93f243c0-b963-9ea0-e053-2995a90aa8522026-01-16WarningsExact identifier
ndc (product): 48951-1318

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1318-14895113180110 AMPULE in 1 BOX (48951-1318-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent