Meteoric Iron Prunus

Product NDC
48951-7052
Requested package NDC
48951-7052-1
11-digit product format
489517052
Labeler code
48951
Product ID
48951-7052_49ef6475-e616-051b-e063-6394a90a0573
Type
HUMAN OTC DRUG
Nonproprietary name
Meteoric Iron Prunus
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ECHINACEA, UNSPECIFIED; IRON; PHOSPHORUS; SILICON DIOXIDE; SLOE
Active strength
3; 12; 6; 12; 2 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Meteoric Iron PrunusMETEORIC IRON PRUNUSUriel Pharmacy Inc.e9020757-2393-4a22-9665-25da0a0993d02026-02-03WarningsExact identifier
ndc (package): 48951-7052-1
ndc (product): 48951-7052
ndc11 (package): 48951705201

Additional Listing Data#

Finished product
Yes
Brand name base
Meteoric Iron Prunus
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SLOE3 [hp_X]/mL
ECHINACEA, UNSPECIFIED12 [hp_X]/mL
PHOSPHORUS6 [hp_X]/mL
IRON12 [hp_X]/mL
SILICON DIOXIDE2 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3MLB4858X7Internal UNII lookup
4N9P6CC1DXInternal UNII lookup
27YLU75U4WInternal UNII lookup
E1UOL152H7Internal UNII lookup
ETJ7Z6XBU4Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
e9020757-2393-4a22-9665-25da0a0993d0Available 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
48951-7052-1Meteoric Iron Prunus10 in 1 BOXLIQUID105
48951-7052-1Meteoric Iron Prunus1 mL in 1 AMPULELIQUID15

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7052METEORIC IRON PRUNUS LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20180529_e9020757-2393-4a22-9665-25da0a0993d0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-7052-14895170520110 AMPULE in 1 BOX (48951-7052-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent