Sinus

Product NDC: 68428-003
11-digit product format: 684280003
Labeler code: 68428
Product ID: 68428-003_9a673a65-fc4e-3d9e-e053-2a95a90ad2f0
Type: HUMAN OTC DRUG
Nonproprietary name: CALCIUM CARBONATE - GOLDENSEAL - POTASSIUM DICHROMATE
Dosage form: PELLET
Route: ORAL
Labeler: Washington Homeopathic Products
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2010-05-12
Marketing end: 0000-00-00
Substance: OYSTER SHELL CALCIUM CARBONATE, CRUDE; GOLDENSEAL; POTASSIUM DICHROMATE
Active strength: 6 [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	68428-003		I	Inactivated by FDA		2026-08-03
excluded package	package	68428-003	68428-003-14	I	Inactivated by FDA		2026-08-03

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	68428-003-14	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	68428-003-14	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	68428-003-14	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	68428-003-14	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	68428-003-14	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	68428-003-14	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	68428-003-14	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	68428-003-14	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	68428-003-14	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
68428-003-14	2025-01-30	C162847	48780-1	2cef2736-9997-d83d-e063-dadaa90ab31f	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68428-003-14	Sinus	28 g in 1 BOTTLE, PLASTIC	PELLET	28		3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CALCIUM CARBONATE	ACTIVE INGREDIENT	H0G9379FGK	SINUS (CALCIUM CARBONATE - GOLDENSEAL - POTASSIUM DICHROMATE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	1
GOLDENSEAL	ACTIVE INGREDIENT	ZW3Z11D0JV	SINUS (CALCIUM CARBONATE - GOLDENSEAL - POTASSIUM DICHROMATE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	1
POTASSIUM DICHROMATE	ACTIVE INGREDIENT	T4423S18FM	SINUS (CALCIUM CARBONATE - GOLDENSEAL - POTASSIUM DICHROMATE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	1
CARBONATE ION	ACTIVE MOIETY	7UJQ5OPE7D	SINUS (CALCIUM CARBONATE - GOLDENSEAL - POTASSIUM DICHROMATE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	1
GOLDENSEAL	ACTIVE MOIETY	ZW3Z11D0JV	SINUS (CALCIUM CARBONATE - GOLDENSEAL - POTASSIUM DICHROMATE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	1
POTASSIUM CATION	ACTIVE MOIETY	295O53K152	SINUS (CALCIUM CARBONATE - GOLDENSEAL - POTASSIUM DICHROMATE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	1
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	SINUS (CALCIUM CARBONATE - GOLDENSEAL - POTASSIUM DICHROMATE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	1
SUCROSE	INACTIVE INGREDIENT	C151H8M554	SINUS (CALCIUM CARBONATE - GOLDENSEAL - POTASSIUM DICHROMATE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68428-003	SINUS (CALCIUM CARBONATE - GOLDENSEAL - POTASSIUM DICHROMATE) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3	Legacy NDC, 1 package rows	20191224_1566e0de-afca-4574-b360-8f4c3e25dc1d.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
2E32821G6I	OYSTER SHELL CALCIUM CARBONATE, CRUDE		OYSTER SHELL CALCIUM CARBONATE, CRUDE
ZW3Z11D0JV	GOLDENSEAL		GOLDENSEAL
T4423S18FM	POTASSIUM DICHROMATE	7778-50-9	POTASSIUM DICHROMATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68428-003-14	68428000314	28 g in 1 BOTTLE, PLASTIC (68428-003-14)	28 g	2010-05-12	0000-00-00	No	No	Current