Be gone Scars

Product NDC: 68428-721
11-digit product format: 684280721
Labeler code: 68428
Product ID: 68428-721_9a5b5ee4-9a51-b68a-e053-2a95a90a182e
Type: HUMAN OTC DRUG
Nonproprietary name: THIOSINAMINUM
Dosage form: OINTMENT
Route: TOPICAL
Labeler: Washington Homeopathic Products
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2013-03-15
Marketing end: 0000-00-00
Substance: ALLYLTHIOUREA
Active strength: 2 [hp_X]/56g
NDC exclude flag: No
Listing certified through: 2020-12-31
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	68428-721		I	Inactivated by FDA		2026-08-17
excluded package	package	68428-721	68428-721-29	I	Inactivated by FDA		2026-08-17

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 · 18 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	68428-721-29	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	68428-721-29	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	68428-721-29	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	68428-721-29	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	68428-721-29	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	68428-721-29	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	68428-721-29	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	68428-721-29	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	68428-721-29	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68428-721-29	2025-01-30	C162847	48780-1	2cef2736-a53c-d83d-e063-dadaa90ab31f	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68428-721-29	Be gone ScarsTM	56 g in 1 TUBE	OINTMENT	56		2

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ALLYLTHIOUREA	ACTIVE INGREDIENT	706IDJ14B7	BE GONE SCARS TM (THIOSINAMINUM) OINTMENT [WASHINGTON HOMEOPATHIC PRODUCTS]	1
ALLYLTHIOUREA	ACTIVE MOIETY	706IDJ14B7	BE GONE SCARS TM (THIOSINAMINUM) OINTMENT [WASHINGTON HOMEOPATHIC PRODUCTS]	1
LANOLIN	INACTIVE INGREDIENT	7EV65EAW6H	BE GONE SCARS TM (THIOSINAMINUM) OINTMENT [WASHINGTON HOMEOPATHIC PRODUCTS]	1
PETROLATUM	INACTIVE INGREDIENT	4T6H12BN9U	BE GONE SCARS TM (THIOSINAMINUM) OINTMENT [WASHINGTON HOMEOPATHIC PRODUCTS]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68428-721	BE GONE SCARS TM (THIOSINAMINUM) OINTMENT [WASHINGTON HOMEOPATHIC PRODUCTS]	2	Legacy NDC, 1 package rows	20191224_019d15fe-6e30-4586-ae12-b4205bedada2.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
706IDJ14B7	ALLYLTHIOUREA	109-57-9	ALLYLTHIOUREA

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68428-721-29	68428072129	56 g in 1 TUBE (68428-721-29)	56 g	2013-03-15	0000-00-00	No	No	Current