FDA.reportPublic FDA data

Pulsatilla

Product NDC
44911-0498
Requested package NDC
44911-0498-1
11-digit product format
449110498
Labeler code
44911
Product ID
44911-0498_e648ebdd-a77d-43b2-ba31-e2dd2d80338c
Type
HUMAN OTC DRUG
Nonproprietary name
Pulsatilla (Pratensis)
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-06-07
Substance
PULSATILLA PRATENSIS WHOLE
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 · 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…
2021-12-27 23:28 UTC · source 2021-12-278dfbde2a14a4…c9ff85d89658…

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PULSATILLA PRATENSIS WHOLE200 [hp_C]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8E272251DIInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
664377e7-2d2f-4a54-bfff-21ff48f7b4eeAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2024-10-29DRUG FACTS:
2024-01-30DRUG FACTS:
2022-03-15DRUG FACTS:
2021-01-29DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0498-1Pulsatilla30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0498PULSATILLA (PULSATILLA (PRATENSIS)) LIQUID [ENERGIQUE, INC.]4Current NDC, Legacy NDC, 1 package rows20241031_664377e7-2d2f-4a54-bfff-21ff48f7b4ee.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
PulsatillaPULSATILLA (PRATENSIS)Energique, Inc.664377e7-2d2f-4a54-bfff-21ff48f7b4ee2024-10-29WarningsExact identifier
ndc (package): 44911-0498-1
ndc (product): 44911-0498
ndc11 (package): 44911049801

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0498-14491104980130 mL in 1 BOTTLE, DROPPER (44911-0498-1) 30 ml2019-06-070000-00-00NoNoCurrent