FDA.reportPublic FDA data

Arnica Power

Product NDC
61096-1032
11-digit product format
610961032
Labeler code
61096
Product ID
61096-1032_1c3e7699-74cd-441a-92f3-d27b8267e8d9
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica montana
Dosage form
LIQUID
Route
ORAL
Labeler
Eight and Company L.L.C
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-03-08
Substance
ARNICA MONTANA WHOLE
Active strength
3 [hp_X]/41mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Arnica Power
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA WHOLE3 [hp_X]/41mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O80TY208ZWInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
48c84c56-1179-4be5-84aa-033ddcb8e80cAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2023-12-14DRUG FACTS:
2023-12-14DRUG FACTS:
2023-12-14Arnica Power
2023-01-30DRUG FACTS:
2023-01-30DRUG FACTS:
2023-01-30Arnica Power
2021-02-09DRUG FACTS:
2021-02-09DRUG FACTS:
2021-02-09Arnica Power
2021-01-29DRUG FACTS:
2021-01-29DRUG FACTS:
2021-01-29Arnica Power

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61096-1032-1Arnica Power1 in 1 CARTONLIQUID18
61096-1032-1Arnica Power41 mL in 1 BOTTLE, SPRAYLIQUID418

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZWSPRAYOLOGY ARNICA POWER 3 (ARNICA MONTANA) LIQUID [EIGHT AND COMPANY]1
ARNICA MONTANAACTIVE MOIETYO80TY208ZWSPRAYOLOGY ARNICA POWER 3 (ARNICA MONTANA) LIQUID [EIGHT AND COMPANY]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MSPRAYOLOGY ARNICA POWER 3 (ARNICA MONTANA) LIQUID [EIGHT AND COMPANY]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXSPRAYOLOGY ARNICA POWER 3 (ARNICA MONTANA) LIQUID [EIGHT AND COMPANY]1
WATERINACTIVE INGREDIENT059QF0KO0RSPRAYOLOGY ARNICA POWER 3 (ARNICA MONTANA) LIQUID [EIGHT AND COMPANY]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61096-1032ARNICA POWER (ARNICA MONTANA) LIQUID [EIGHT AND COMPANY L.L.C]6Current NDC, Legacy NDC, 2 package rows20250110_48c84c56-1179-4be5-84aa-033ddcb8e80c.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 PowerARNICA MONTANAEight and Company L.L.C48c84c56-1179-4be5-84aa-033ddcb8e80c2025-12-18WarningsExact identifier
ndc (product): 61096-1032

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
61096-1032-1610961032011 BOTTLE, SPRAY in 1 CARTON (61096-1032-1) / 41 mL in 1 BOTTLE, SPRAY2019-03-080000-00-00NoNoCurrent