Fungus

Product NDC: 68428-009
11-digit product format: 684280009
Labeler code: 68428
Product ID: 68428-009_9a67d130-efc3-5822-e053-2a95a90afe04
Type: HUMAN OTC DRUG
Nonproprietary name: GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG
Dosage form: PELLET
Route: ORAL
Labeler: Washington Homeopathic Products
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2010-07-07
Marketing end: 0000-00-00
Substance: GRAPHITE; SEPIA OFFICINALIS JUICE; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG
Active strength: 6 [hp_C]/28g; [hp_C]/28g; [hp_C]/28g; [hp_C]/28g
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	68428-009		I	Inactivated by FDA		2026-10-12
excluded package	package	68428-009	68428-009-14	I	Inactivated by FDA		2026-10-12

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	68428-009-14	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	68428-009-14	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	68428-009-14	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	68428-009-14	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	68428-009-14	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	68428-009-14	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	68428-009-14	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	68428-009-14	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	68428-009-14	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68428-009-14	2025-01-30	C162847	48780-1	2cef2736-5b07-d83d-e063-dadaa90ab31f	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68428-009-14	Fungus	28 g in 1 BOTTLE, PLASTIC	PELLET	28		5

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
GRAPHITE	ACTIVE INGREDIENT	4QQN74LH4O	FUNGUS (GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3
SEPIA OFFICINALIS JUICE	ACTIVE INGREDIENT	QDL83WN8C2	FUNGUS (GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3
SULFUR	ACTIVE INGREDIENT	70FD1KFU70	FUNGUS (GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3
THUJA OCCIDENTALIS LEAFY TWIG	ACTIVE INGREDIENT	1NT28V9397	FUNGUS (GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3
GRAPHITE	ACTIVE MOIETY	4QQN74LH4O	FUNGUS (GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3
SEPIA OFFICINALIS JUICE	ACTIVE MOIETY	QDL83WN8C2	FUNGUS (GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3
SULFUR	ACTIVE MOIETY	70FD1KFU70	FUNGUS (GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3
THUJA OCCIDENTALIS LEAFY TWIG	ACTIVE MOIETY	1NT28V9397	FUNGUS (GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	FUNGUS (GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3
SUCROSE	INACTIVE INGREDIENT	C151H8M554	FUNGUS (GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68428-009	FUNGUS (GRAPHITE - SEPIA OFFICINALIS JUICE - SULFUR - THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	5	Legacy NDC, 1 package rows	20191224_ba4c9f5f-4767-46fb-b11f-b1b6d18493a8.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4QQN74LH4O	GRAPHITE	7782-42-5	GRAPHITE
QDL83WN8C2	SEPIA OFFICINALIS JUICE		SEPIA OFFICINALIS JUICE
70FD1KFU70	SULFUR	7704-34-9	SULFUR
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
68428-009-14	68428000914	28 g in 1 BOTTLE, PLASTIC (68428-009-14)	28 g	2010-07-07	0000-00-00	No	No	Current