Equisetum Viscum

Product NDC
48951-4042
11-digit product format
489514042
Labeler code
48951
Product ID
48951-4042_5388aac4-7671-0f23-e063-6394a90a0325
Type
HUMAN OTC DRUG
Nonproprietary name
Equisetum Viscum
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
EQUISETUM ARVENSE TOP; PORK KIDNEY; VISCUM ALBUM FRUITING TOP
Active strength
6; 6; 6 [hp_X]/mL; [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 Viscum
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
EQUISETUM ARVENSE TOP6 [hp_X]/mL
PORK KIDNEY6 [hp_X]/mL
VISCUM ALBUM FRUITING TOP6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1DP6Y6B65ZInternal UNII lookup
X7BCI5P86HInternal UNII lookup
BK9092J5MPInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
86f00045-97c7-4029-b7ab-420696f041d2Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4042-1Equisetum Viscum1 mL in 1 AMPULELIQUID14
48951-4042-1Equisetum Viscum10 in 1 BOXLIQUID104

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65ZEQUISETUM VISCUM LIQUID [URIEL PHARMACY INC.]1
PORK KIDNEYACTIVE INGREDIENTX7BCI5P86HEQUISETUM VISCUM LIQUID [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPEQUISETUM VISCUM LIQUID [URIEL PHARMACY INC.]1
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65ZEQUISETUM VISCUM LIQUID [URIEL PHARMACY INC.]1
PORK KIDNEYACTIVE MOIETYX7BCI5P86HEQUISETUM VISCUM LIQUID [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPEQUISETUM VISCUM LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XEQUISETUM VISCUM LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0REQUISETUM VISCUM LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4042EQUISETUM VISCUM LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20240410_86f00045-97c7-4029-b7ab-420696f041d2.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 ViscumEQUISETUM VISCUMUriel Pharmacy Inc.86f00045-97c7-4029-b7ab-420696f041d22026-06-05WarningsExact identifier
ndc (product): 48951-4042

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-4042-14895140420110 AMPULE in 1 BOX (48951-4042-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent