FDA.reportPublic FDA data

Aurum Ferrum sidereum comp.

Product NDC
48951-1395
11-digit product format
489511395
Labeler code
48951
Product ID
48951-1395_2d7a181a-a1b9-f475-e063-6294a90a8021
Type
HUMAN OTC DRUG
Nonproprietary name
Aurum Ferrum sidereum comp.
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ANTIMONY; GOLD; IRON; KALANCHOE DAIGREMONTIANA LEAF
Active strength
8; 10; 10; 2 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Aurum Ferrum sidereum comp.
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANTIMONY8 [hp_X]/mL
GOLD10 [hp_X]/mL
IRON10 [hp_X]/mL
KALANCHOE DAIGREMONTIANA LEAF2 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9IT35J3UV3, 79Y1949PYO, E1UOL152H7, L6X13JKL8O

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1395-3Aurum Ferrum sidereum comp.60 mL in 1 BOTTLE, DROPPERLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1395AURUM FERRUM SIDEREUM COMP. LIQUID [URIEL PHARMACY, INC]1Current NDC, 1 package rows20250209_2d7a181a-a1b8-f475-e063-6294a90a8021.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
48951-1395-34895113950360 mL in 1 BOTTLE, DROPPER (48951-1395-3) 60 ml2009-09-01NoNoCurrent