FDA.reportPublic FDA data

Arnica Aconitum

Product NDC
48951-1103
11-digit product format
489511103
Labeler code
48951
Product ID
48951-1103_43585b42-4c42-eba6-e063-6394a90abbfb
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Aconitum
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ARNICA MONTANA FLOWER; BETULA PUBESCENS LEAF; MANDRAGORA OFFICINARUM ROOT; ACONITUM NAPELLUS
Active strength
1; 2; 2; 4 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
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
Arnica Aconitum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA FLOWER1 [hp_X]/1
BETULA PUBESCENS LEAF2 [hp_X]/1
MANDRAGORA OFFICINARUM ROOT2 [hp_X]/1
ACONITUM NAPELLUS4 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
OZ0E5Y15PZInternal UNII lookup
84SOH0O3OOInternal UNII lookup
I2XCB174VBInternal UNII lookup
U0NQ8555JDInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
ba2a81b4-9efc-4706-9330-97475a27dc82Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1103-2Arnica Aconitum1350 in 1 BOTTLE, GLASSPELLET13504

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACONITUM NAPELLUSACTIVE INGREDIENTU0NQ8555JDARNICA ACONITUM PELLET [URIEL PHARMACY INC.]1
ARNICA MONTANA FLOWERACTIVE INGREDIENTOZ0E5Y15PZARNICA ACONITUM PELLET [URIEL PHARMACY INC.]1
BETULA PUBESCENS LEAFACTIVE INGREDIENT84SOH0O3OOARNICA ACONITUM PELLET [URIEL PHARMACY INC.]1
MANDRAGORA OFFICINARUM ROOTACTIVE INGREDIENTI2XCB174VBARNICA ACONITUM PELLET [URIEL PHARMACY INC.]1
ACONITUM NAPELLUSACTIVE MOIETYU0NQ8555JDARNICA ACONITUM PELLET [URIEL PHARMACY INC.]1
ARNICA MONTANA FLOWERACTIVE MOIETYOZ0E5Y15PZARNICA ACONITUM PELLET [URIEL PHARMACY INC.]1
BETULA PUBESCENS LEAFACTIVE MOIETY84SOH0O3OOARNICA ACONITUM PELLET [URIEL PHARMACY INC.]1
MANDRAGORA OFFICINARUM ROOTACTIVE MOIETYI2XCB174VBARNICA ACONITUM PELLET [URIEL PHARMACY INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ARNICA ACONITUM PELLET [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1103ARNICA ACONITUM PELLET [URIEL PHARMACY INC.]3Current NDC, Legacy NDC, 1 package rows20180531_ba2a81b4-9efc-4706-9330-97475a27dc82.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
Arnica AconitumARNICA ACONITUMUriel Pharmacy Inc.ba2a81b4-9efc-4706-9330-97475a27dc822025-11-11WarningsExact identifier
ndc (product): 48951-1103

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1103-2489511103021350 PELLET in 1 BOTTLE, GLASS (48951-1103-2) 1350 pellet2009-09-010000-00-00NoNoCurrent