Coniferyl Alcohol Phenolic

Product NDC
44911-0253
Requested package NDC
44911-0253-1
11-digit product format
449110253
Labeler code
44911
Product ID
44911-0253_fb7b94f9-e1de-429b-9bea-71ffd71c0946
Type
HUMAN OTC DRUG
Nonproprietary name
Coniferyl Alcohol
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-08-31
Substance
CONIFERYL ALCOHOL
Active strength
6 [hp_X]/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 · 5 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…

Additional Listing Data#

Finished product
Yes
Brand name base
Coniferyl Alcohol Phenolic
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CONIFERYL ALCOHOL6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
E7SM92591PInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
1f65cd4e-21ce-4e78-9950-fb4f70554e02Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2024-10-24DRUG FACTS:
2023-01-30DRUG FACTS:
2021-05-17DRUG FACTS:
2021-01-29DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0253-1Coniferyl Alcohol Phenolic30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0253CONIFERYL ALCOHOL PHENOLIC (CONIFERYL ALCOHOL) LIQUID [ENERGIQUE, INC.]4Current NDC, Legacy NDC, 1 package rows20241027_1f65cd4e-21ce-4e78-9950-fb4f70554e02.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
Coniferyl Alcohol PhenolicCONIFERYL ALCOHOLEnergique, Inc.1f65cd4e-21ce-4e78-9950-fb4f70554e022024-10-24WarningsExact identifier
ndc (package): 44911-0253-1
ndc (product): 44911-0253
ndc11 (package): 44911025301

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0253-14491102530130 mL in 1 BOTTLE, DROPPER (44911-0253-1) 30 ml2015-08-310000-00-00NoNoCurrent