Home NDC 50169-0002 Type 3 Sinus Regular
Product NDC 50169-0002
11-digit product format 501690002
Labeler code 50169
Product ID 50169-0002_0cbdfc87-59a1-477a-b0ce-5f3ad0a20d69
Type HUMAN OTC DRUG
Nonproprietary name Silicea, Hydrastis Canadensis, Kali Bichromicum, Calcarea Carbonica
Dosage form TABLET, ORALLY DISINTEGRATING
Route ORAL
Labeler T Gone Remedies
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2013-04-03
Marketing end 0000-00-00
Substance SILICON DIOXIDE; GOLDENSEAL; POTASSIUM DICHROMATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE
Active strength 6 [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg
NDC exclude flag No
Listing certified through 2019-12-31
Current FDA listing Historical FDA.report record 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 · 42 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 50169-0002-1 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 50169-0002-1 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 50169-0002-1 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 50169-0002-1 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 50169-0002-1 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 50169-0002-1 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 50169-0002-1 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 50169-0002-1 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 50169-0002-1 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 50169-0002-1 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 50169-0002-1 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 50169-0002-1 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 50169-0002-1 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 50169-0002-1 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 50169-0002-1 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 50169-0002-1 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 50169-0002-1 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 50169-0002-1 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 50169-0002-1 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 50169-0002-1 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 50169-0002-1 9bebd1f3094a…5416666fcb17…
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50169-0002-1 Type 3 Sinus Regular 15000 mg in 1 BOTTLE TABLET, ORALLY DISINTEGRATING 15000 1
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded GOLDENSEAL ACTIVE INGREDIENT ZW3Z11D0JV TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1 OYSTER SHELL CALCIUM CARBONATE, CRUDE ACTIVE INGREDIENT 2E32821G6I TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1 POTASSIUM DICHROMATE ACTIVE INGREDIENT T4423S18FM TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1 SILICON DIOXIDE ACTIVE INGREDIENT ETJ7Z6XBU4 TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1 COLLOIDAL SILICON DIOXIDE ACTIVE MOIETY ETJ7Z6XBU4 TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1 DICHROMATE ION ACTIVE MOIETY 9LKY4BFN2V TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1 GOLDENSEAL ACTIVE MOIETY ZW3Z11D0JV TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1 OYSTER SHELL CALCIUM CARBONATE, CRUDE ACTIVE MOIETY 2E32821G6I TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1 LACTOSE INACTIVE INGREDIENT J2B2A4N98G TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50169-0002 TYPE 3 SINUS REGULAR (SILICEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, CALCAREA CARBONICA) TABLET, ORALLY DISINTEGRATING [T GONE REMEDIES] 1 Legacy NDC, 1 package rows 20130413_ff9fa888-d00a-4df0-bece-ea5e573fe6fd.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Status 50169-0002-1 50169000201 15000 mg in 1 BOTTLE 15000 mg Historical