Ferrum rosatum Graphites

Product NDC
48951-4064
11-digit product format
489514064
Labeler code
48951
Product ID
48951-4064_3893ba53-bc49-2646-e063-6294a90aed82
Type
HUMAN OTC DRUG
Nonproprietary name
Ferrum rosatum Graphites
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
SEDUM ROSEUM WHOLE; FERRIC OXIDE RED; IRON; GRAPHITE
Active strength
3; 3; 6; 17 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
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
Ferrum rosatum Graphites
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SEDUM ROSEUM WHOLE3 [hp_X]/mL
FERRIC OXIDE RED3 [hp_X]/mL
IRON6 [hp_X]/mL
GRAPHITE17 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
RH0WP583U3Internal UNII lookup
1K09F3G675Internal UNII lookup
E1UOL152H7Internal UNII lookup
4QQN74LH4OInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
1a4ca338-eada-4c0f-8bce-480244940c89Available 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
48951-4064-3Ferrum rosatum Graphites60 mL in 1 BOTTLE, DROPPERLIQUID605

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4064FERRUM ROSATUM GRAPHITES LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 1 package rows20180426_1a4ca338-eada-4c0f-8bce-480244940c89.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
Ferrum rosatum GraphitesFERRUM ROSATUM GRAPHITESUriel Pharmacy Inc.1a4ca338-eada-4c0f-8bce-480244940c892025-06-27WarningsExact identifier
ndc (product): 48951-4064

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-4064-34895140640360 mL in 1 BOTTLE, DROPPER (48951-4064-3) 60 ml2009-09-010000-00-00NoNoCurrent