Aconitum Napellus 200C

Product NDC
43406-0159
11-digit product format
434060159
Labeler code
43406
Product ID
43406-0159_af011067-478f-4d5e-8e3f-d98864508175
Type
HUMAN OTC DRUG
Nonproprietary name
Aconitum Napellus
Dosage form
LIQUID
Route
ORAL
Labeler
Natural Creations, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-02-26
Substance
ACONITUM NAPELLUS
Active strength
200 [hp_C]/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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2021-12-27 23:28 UTC · source 2021-12-27excluded productproduct43406-0159IInactivated by FDAexcluded / ndc_excluded.zip8dfbde2a14a4…c9ff85d89658…
2021-12-27 23:28 UTC · source 2021-12-27excluded packagepackage43406-015943406-0159-1IInactivated by FDAexcluded / ndc_excluded.zip8dfbde2a14a4…c9ff85d89658…

Additional Listing Data#

Finished product
Yes
Brand name base
Aconitum Napellus 200C
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM NAPELLUS200 [hp_C]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
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
91f429ad-10ef-45e0-b7f8-3c254d873cb5Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0159-12022-02-14C16284748780-1ba0f9c33-202a-a910-e053-dadaa90a0b85Aconitum Napellus 200C
43406-0159-12021-01-29C16284748780-1ba0f9c33-202a-a910-e053-dadaa90a0b85Aconitum Napellus 200C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0159-1Aconitum Napellus 200C30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43406-0159ACONITUM NAPELLUS 200C (ACONITUM NAPELLUS) LIQUID [NATURAL CREATIONS, INC]2Current NDC, Legacy NDC, 1 package rows20220215_91f429ad-10ef-45e0-b7f8-3c254d873cb5.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
Aconitum Napellus 200CACONITUM NAPELLUSNatural Creations, Inc91f429ad-10ef-45e0-b7f8-3c254d873cb52022-02-14WarningsExact identifier
ndc (product): 43406-0159

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43406-0159-14340601590130 mL in 1 BOTTLE, DROPPER (43406-0159-1) 30 ml2013-02-260000-00-00NoNoCurrent