FDA.reportPublic FDA data

Renes Veratrum

Product NDC
48951-8133
11-digit product format
489518133
Labeler code
48951
Product ID
48951-8133_3eef890d-751b-d952-e063-6294a90a4036
Type
HUMAN OTC DRUG
Nonproprietary name
Renes Veratrum
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
APIS MELLIFERA; EQUISETUM ARVENSE TOP; PORK KIDNEY; VERATRUM ALBUM ROOT; VISCUM ALBUM FRUITING TOP
Active strength
30; 20; 7; 6; 20 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes
Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Renes Veratrum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
VERATRUM ALBUM ROOT30 [hp_X]/1
PORK KIDNEY20 [hp_X]/1
EQUISETUM ARVENSE TOP7 [hp_X]/1
VISCUM ALBUM FRUITING TOP6 [hp_X]/1
APIS MELLIFERA20 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
QNS6W5US1ZInternal UNII lookup
X7BCI5P86HInternal UNII lookup
1DP6Y6B65ZInternal UNII lookup
BK9092J5MPInternal UNII lookup
7S82P3R43ZInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
92209110-eb47-42de-831a-c35a72ef2fd2Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8133-2Renes Veratrum1350 in 1 BOTTLE, GLASSPELLET13504

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43ZRENES VERATRUM PELLET [URIEL PHARMACY INC.]1
EQUISETUM ARVENSE TOPACTIVE INGREDIENT1DP6Y6B65ZRENES VERATRUM PELLET [URIEL PHARMACY INC.]1
PORK KIDNEYACTIVE INGREDIENTX7BCI5P86HRENES VERATRUM PELLET [URIEL PHARMACY INC.]1
VERATRUM ALBUM ROOTACTIVE INGREDIENTQNS6W5US1ZRENES VERATRUM PELLET [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPRENES VERATRUM PELLET [URIEL PHARMACY INC.]1
APIS MELLIFERAACTIVE MOIETY7S82P3R43ZRENES VERATRUM PELLET [URIEL PHARMACY INC.]1
EQUISETUM ARVENSE TOPACTIVE MOIETY1DP6Y6B65ZRENES VERATRUM PELLET [URIEL PHARMACY INC.]1
PORK KIDNEYACTIVE MOIETYX7BCI5P86HRENES VERATRUM PELLET [URIEL PHARMACY INC.]1
VERATRUM ALBUM ROOTACTIVE MOIETYQNS6W5US1ZRENES VERATRUM PELLET [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPRENES VERATRUM PELLET [URIEL PHARMACY INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554RENES VERATRUM PELLET [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8133RENES VERATRUM PELLET [URIEL PHARMACY INC.]3Current NDC, Legacy NDC, 1 package rows20180606_92209110-eb47-42de-831a-c35a72ef2fd2.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
Renes VeratrumRENES VERATRUMUriel Pharmacy Inc.92209110-eb47-42de-831a-c35a72ef2fd22025-09-16WarningsExact identifier
ndc (product): 48951-8133

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8133-2489518133021350 PELLET in 1 BOTTLE, GLASS (48951-8133-2) 1350 pellet2009-09-010000-00-00NoNoCurrent