Anise Pyrite

Product NDC
48951-1036
11-digit product format
489511036
Labeler code
48951
Product ID
48951-1036_2c531a5c-bddb-6430-e063-6294a90ad39f
Type
HUMAN OTC DRUG
Nonproprietary name
Anise Pyrite
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ANISE; FERROUS DISULFIDE; SUCROSE
Active strength
3; 3; 3 [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
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
Anise Pyrite
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ANISE3 [hp_X]/1
FERROUS DISULFIDE3 [hp_X]/1
SUCROSE3 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
21C2F5E8REInternal UNII lookup
132N09W4PRInternal UNII lookup
C151H8M554Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
a03cdeb0-8347-40cc-8d17-5510d99575c7Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1036-2Anise Pyrite1350 in 1 BOTTLE, GLASSPELLET13506

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ANISEACTIVE INGREDIENT21C2F5E8REANISE PYRITE PELLET [URIEL PHARMACY INC.]1
FERROUS DISULFIDEACTIVE INGREDIENT132N09W4PRANISE PYRITE PELLET [URIEL PHARMACY INC.]1
SUCROSEACTIVE INGREDIENTC151H8M554ANISE PYRITE PELLET [URIEL PHARMACY INC.]1
ANISEACTIVE MOIETY21C2F5E8REANISE PYRITE PELLET [URIEL PHARMACY INC.]1
FERROUS CATIONACTIVE MOIETYGW89581OWRANISE PYRITE PELLET [URIEL PHARMACY INC.]1
SUCROSEACTIVE MOIETYC151H8M554ANISE PYRITE PELLET [URIEL PHARMACY INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GANISE PYRITE PELLET [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1036ANISE PYRITE PELLET [URIEL PHARMACY INC.]6Current NDC, Legacy NDC, 1 package rows20250124_a03cdeb0-8347-40cc-8d17-5510d99575c7.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
Anise PyriteANISE PYRITEUriel Pharmacy Inc.a03cdeb0-8347-40cc-8d17-5510d99575c72025-01-22WarningsExact identifier
ndc (product): 48951-1036

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1036-2489511036021350 PELLET in 1 BOTTLE, GLASS (48951-1036-2) 1350 pellet2009-09-010000-00-00NoNoCurrent