Home NDC 59262-240 Sinus Relief
Product NDC 59262-240
11-digit product format 592620240
Labeler code 59262
Product ID 59262-240_e7022d4f-c1d3-4a94-88d3-8ff9fffde6ef
Type HUMAN OTC DRUG
Nonproprietary name Kali bichromicum, Luffa operculata, Sabadilla
Dosage form SPRAY
Route NASAL
Labeler Similasan Corporation
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2013-07-02
Marketing end 0000-00-00
Substance LUFFA OPERCULATA FRUIT; POTASSIUM DICHROMATE; SCHOENOCAULON OFFICINALE SEED
Active strength 6 [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL
NDC exclude flag No
Listing certified through 2024-12-31
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 · 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 59262-240-20 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 59262-240-20 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 59262-240-20 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 59262-240-20 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 59262-240-20 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 59262-240-20 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 59262-240-20 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 59262-240-20 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 59262-240-20 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# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59262-240-20 Sinus Relief 20 mL in 1 BOTTLE, SPRAY SPRAY 20 10
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded LUFFA OPERCULATA FRUIT ACTIVE INGREDIENT C4MO6809HU SINUS RELIEF (KALI BICHROMICUM, LUFFA OPERCULATA, SABADILLA) SPRAY [SIMILASAN CORPORATION] 6 POTASSIUM DICHROMATE ACTIVE INGREDIENT T4423S18FM SINUS RELIEF (KALI BICHROMICUM, LUFFA OPERCULATA, SABADILLA) SPRAY [SIMILASAN CORPORATION] 6 SCHOENOCAULON OFFICINALE SEED ACTIVE INGREDIENT 6NAF1689IO SINUS RELIEF (KALI BICHROMICUM, LUFFA OPERCULATA, SABADILLA) SPRAY [SIMILASAN CORPORATION] 6 LUFFA OPERCULATA FRUIT ACTIVE MOIETY C4MO6809HU SINUS RELIEF (KALI BICHROMICUM, LUFFA OPERCULATA, SABADILLA) SPRAY [SIMILASAN CORPORATION] 6 POTASSIUM CATION ACTIVE MOIETY 295O53K152 SINUS RELIEF (KALI BICHROMICUM, LUFFA OPERCULATA, SABADILLA) SPRAY [SIMILASAN CORPORATION] 6 SCHOENOCAULON OFFICINALE SEED ACTIVE MOIETY 6NAF1689IO SINUS RELIEF (KALI BICHROMICUM, LUFFA OPERCULATA, SABADILLA) SPRAY [SIMILASAN CORPORATION] 6 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X SINUS RELIEF (KALI BICHROMICUM, LUFFA OPERCULATA, SABADILLA) SPRAY [SIMILASAN CORPORATION] 6 WATER INACTIVE INGREDIENT 059QF0KO0R SINUS RELIEF (KALI BICHROMICUM, LUFFA OPERCULATA, SABADILLA) SPRAY [SIMILASAN CORPORATION] 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59262-240 SINUS RELIEF (KALI BICHROMICUM, LUFFA OPERCULATA, SABADILLA) SPRAY [SIMILASAN CORPORATION] 10 Legacy NDC, 1 package rows 20230106_52142c94-c724-414c-88df-258b58ceaf25.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59262-240-20 59262024020 20 mL in 1 BOTTLE, SPRAY (59262-240-20) 20 ml 2013-07-02 0000-00-00 No No Current