Arnica

Product NDC
44911-0218
Requested package NDC
44911-0218-1
11-digit product format
449110218
Labeler code
44911
Product ID
44911-0218_d65146c8-eb30-44ed-a1e3-7a12f4b77d25
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Montana
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-07-15
Substance
ARNICA MONTANA WHOLE
Active strength
30 wk/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-288af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-081332a3947898…d4bfe170f9cd…
2020-06-10 20:45 UTC · source 2020-06-109bebd1f3094a…5416666fcb17…

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA WHOLE30 wk/mL

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
616e40d9-b1f0-4d17-b739-b548785cb34bAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2024-10-24DRUG FACTS:
2024-01-30DRUG FACTS:
2020-06-26DRUG FACTS:
2020-01-31DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0218-1Arnica30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZWARNICA (ARNICA MONTANA) LIQUID [ENERGIQUE, INC.]1
ARNICA MONTANAACTIVE MOIETYO80TY208ZWARNICA (ARNICA MONTANA) LIQUID [ENERGIQUE, INC.]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MARNICA (ARNICA MONTANA) LIQUID [ENERGIQUE, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RARNICA (ARNICA MONTANA) LIQUID [ENERGIQUE, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0218ARNICA (ARNICA MONTANA) LIQUID [ENERGIQUE, INC.]5Current NDC, Legacy NDC, 1 package rows20241027_616e40d9-b1f0-4d17-b739-b548785cb34b.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
ArnicaARNICA MONTANAEnergique, Inc.616e40d9-b1f0-4d17-b739-b548785cb34b2024-10-24WarningsExact identifier
ndc (package): 44911-0218-1
ndc (product): 44911-0218
ndc11 (package): 44911021801

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0218-14491102180130 mL in 1 BOTTLE, DROPPER (44911-0218-1) 30 ml2015-07-150000-00-00NoNoCurrent