Drosera

Product NDC: 53645-2000
11-digit product format: 536452000
Labeler code: 53645
Product ID: 53645-2000_f03250ea-5f9c-79c8-e053-2995a90a5faf
Type: HUMAN OTC DRUG
Nonproprietary name: Drosera
Dosage form: GLOBULE
Route: ORAL
Labeler: True Botanica, LLC
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2014-02-03
Marketing end: 0000-00-00
Substance: DROSERA INTERMEDIA
Active strength: 6 [hp_X]/23g
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	53645-2000		D	Discontinued by firm		2026-08-07
excluded package	package	53645-2000	53645-2000-3	D	Discontinued by firm		2026-08-07

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 · 12 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	53645-2000-3	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	53645-2000-3	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	53645-2000-3	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	53645-2000-3	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	53645-2000-3	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	53645-2000-3	`cdf11ea48f46…`	`ba0047e9e063…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53645-2000-3	2021-01-31	C162847	48780-1	ba0f9c33-2aeb-a910-e053-dadaa90a0b85	Drosera 6X
53645-2000-3	2021-01-29	C162847	48780-1	ba0f9c33-2aeb-a910-e053-dadaa90a0b85	Drosera 6X

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
B3G4A96QLY	DROSERA INTERMEDIA	DROSERA INTERMEDIA

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
53645-2000-3	53645200003	23 g in 1 BOTTLE (53645-2000-3)	23 g	2014-02-03	0000-00-00	No	No	Current

Drosera

NDC auxiliary status#

Observed NDC auxiliary status history#

FDA-Initiated Inactive NDC Indexing#

Related Records#

Related UNII Ingredients#

Packages#

Related DailyMed Labels#