Equisetum Silicea

Product NDC
48951-4039
11-digit product format
489514039
Labeler code
48951
Product ID
48951-4039_4e43eb39-76aa-f806-e063-6394a90af572
Type
HUMAN OTC DRUG
Nonproprietary name
Equisetum Silicea
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
EQUISETUM ARVENSE TOP; SILICON DIOXIDE
Active strength
3; 3 [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2027-12-31
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
Equisetum Silicea
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
EQUISETUM ARVENSE TOP3 [hp_X]/mL
SILICON DIOXIDE3 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1DP6Y6B65ZInternal 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
e88b820b-4a07-42e2-8fe2-b30729e91a8cAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4039-3Equisetum Silicea60 mL in 1 BOTTLE, DROPPERLIQUID605

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
COLLOIDAL SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU4EQUISETUM SILICEA LIQUID [URIEL PHARMACY INC.]1
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65ZEQUISETUM SILICEA LIQUID [URIEL PHARMACY INC.]1
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU4EQUISETUM SILICEA LIQUID [URIEL PHARMACY INC.]1
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65ZEQUISETUM SILICEA LIQUID [URIEL PHARMACY INC.]1
PROPOLIS WAXINACTIVE INGREDIENT6Y8XYV2NOFEQUISETUM SILICEA LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0REQUISETUM SILICEA LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4039EQUISETUM SILICEA LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 1 package rows20240206_e88b820b-4a07-42e2-8fe2-b30729e91a8c.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
Equisetum SiliceaEQUISETUM SILICEAUriel Pharmacy Inc.e88b820b-4a07-42e2-8fe2-b30729e91a8c2026-03-30WarningsExact identifier
ndc (product): 48951-4039

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-4039-34895140390360 mL in 1 BOTTLE, DROPPER (48951-4039-3) 60 ml2009-09-010000-00-00NoNoCurrent