Sepia

Product NDC: 44911-0391
11-digit product format: 449110391
Labeler code: 44911
Product ID: 44911-0391_20916d43-d6d9-4838-b58b-b78d271e0337
Type: HUMAN OTC DRUG
Nonproprietary name: Sepia
Dosage form: LIQUID
Route: ORAL
Labeler: Energique, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2016-08-22
Substance: SEPIA OFFICINALIS JUICE
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 date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product	44911-0391		I	Inactivated by FDA		excluded / ndc_excluded.zip	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	44911-0391	44911-0391-1	I	Inactivated by FDA		excluded / ndc_excluded.zip	`8dfbde2a14a4…`	`c9ff85d89658…`

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SEPIA OFFICINALIS JUICE	200 [hp_C]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
QDL83WN8C2	Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
02506ea3-276b-452e-8477-ca49b329a3b8	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
44911-0391-1	2022-03-15	C162847	48780-1	ba0f9c33-25f0-a910-e053-dadaa90a0b85	DRUG FACTS:
44911-0391-1	2021-01-29	C162847	48780-1	ba0f9c33-25f0-a910-e053-dadaa90a0b85	DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
44911-0391-1	Sepia	30 mL in 1 BOTTLE, DROPPER	LIQUID	30		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
44911-0391	SEPIA LIQUID [ENERGIQUE, INC.]	5	Current NDC, Legacy NDC, 1 package rows	20250430_02506ea3-276b-452e-8477-ca49b329a3b8.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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sepia	SEPIA	Energique, Inc.	02506ea3-276b-452e-8477-ca49b329a3b8	2025-04-29	Warnings	Exact identifier ndc (product): 44911-0391

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
QDL83WN8C2	SEPIA OFFICINALIS JUICE	SEPIA OFFICINALIS JUICE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
44911-0391-1	44911039101	30 mL in 1 BOTTLE, DROPPER (44911-0391-1)	30 ml	2016-08-22	0000-00-00	No	No	Current