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
KALANCHOE DAIGREMONTIANA LEAF; ANTIMONY; IRON; GOLD
Active strength
2; 8; 10; 10 [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

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

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

Active Ingredients#

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

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L6X13JKL8OInternal UNII lookup
9IT35J3UV3Internal UNII lookup
E1UOL152H7Internal UNII lookup
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
2d7a181a-a1b8-f475-e063-6294a90a8021Available on FDA.report

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

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 Ferrum sidereum comp.AURUM FERRUM SIDEREUM COMP.Uriel Pharmacy, Inc2d7a181a-a1b8-f475-e063-6294a90a80212025-02-06WarningsExact identifier
ndc (product): 48951-1395

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