Thuja

Product NDC: 44911-0156
Requested package NDC: 44911-0156-1
11-digit product format: 449110156
Labeler code: 44911
Product ID: 44911-0156_4906610c-6c3c-4086-80f1-08f49052811b
Type: HUMAN OTC DRUG
Nonproprietary name: Thuja Occidentalis
Dosage form: LIQUID
Route: ORAL
Labeler: Energique, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2015-05-14
Marketing end: 2026-06-11
Substance: THUJA OCCIDENTALIS LEAFY TWIG
Active strength: 30 [hp_C]/mL
NDC exclude flag: No
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	44911-0156	44911-0156-1	D	Discontinued by firm		2026-08-10

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 · 1 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
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	44911-0156	44911-0156-1	I	Inactivated by FDA		excluded / ndc_excluded.zip	`9bebd1f3094a…`	`5416666fcb17…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
44911-0156-1	2020-06-29	C162847	48780-1	9d75b9d0-f634-f424-e053-dadaa90a57ce	DRUG FACTS:
44911-0156-1	2020-01-31	C162847	48780-1	9d75b9d0-f634-f424-e053-dadaa90a57ce	DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
44911-0156-1	Thuja	30 mL in 1 BOTTLE, DROPPER	LIQUID	30		4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
THUJA OCCIDENTALIS LEAFY TWIG	ACTIVE INGREDIENT	1NT28V9397	THUJA (THUJA OCCIDENTALIS) LIQUID [ENERGIQUE, INC.]	1
THUJA OCCIDENTALIS LEAFY TWIG	ACTIVE MOIETY	1NT28V9397	THUJA (THUJA OCCIDENTALIS) LIQUID [ENERGIQUE, INC.]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	THUJA (THUJA OCCIDENTALIS) LIQUID [ENERGIQUE, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	THUJA (THUJA OCCIDENTALIS) LIQUID [ENERGIQUE, INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
44911-0156	THUJA (THUJA OCCIDENTALIS) LIQUID [ENERGIQUE, INC.]	4	Current NDC, Legacy NDC, 1 package rows	20220701_25ec51fc-c898-4cbc-a579-57c5e9514a34.zip

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
1NT28V9397	THUJA OCCIDENTALIS LEAFY TWIG	THUJA OCCIDENTALIS LEAFY TWIG

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
44911-0156-1	44911015601	30 mL in 1 BOTTLE, DROPPER (44911-0156-1)	30 ml	2015-05-14	2026-06-11	No	No	Current