Home NDC 59262-275 Ear Ringing Remedy
Product NDC 59262-275
11-digit product format 592620275
Labeler code 59262
Product ID 59262-275_5c3a1e6f-a15d-4fc7-e063-6394a90ae657
Type HUMAN OTC DRUG
Nonproprietary name ALLYLTHIOUREA, ARNICA MONTANA FLOWER, CALCIUM SULFIDE, ERIODICTYON CALIFORNICUM LEAF, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, QUININE SULFATE, SILICA DIMETHYL SILYLATE
Dosage form SOLUTION
Route AURICULAR (OTIC)
Labeler Similasan Corporation
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2018-01-01
Substance ARNICA MONTANA FLOWER; QUININE SULFATE; ERIODICTYON CALIFORNICUM LEAF; CALCIUM SULFIDE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; SILICA DIMETHYL SILYLATE; ALLYLTHIOUREA
Active strength 15; 12; 12; 12; 15; 12; 15; 15 [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL
Pharmacologic classes Antimalarial [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 · 22 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 59262-275-11 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 59262-275-11 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 59262-275-11 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 59262-275-11 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 59262-275-11 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 59262-275-11 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 59262-275-11 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 59262-275-11 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 59262-275-11 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 59262-275-11 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 59262-275-11 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Ear Ringing Remedy
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA FLOWER 15 [hp_X]/10mL QUININE SULFATE 12 [hp_X]/10mL ERIODICTYON CALIFORNICUM LEAF 12 [hp_X]/10mL CALCIUM SULFIDE 12 [hp_X]/10mL LACHESIS MUTA VENOM 15 [hp_X]/10mL LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/10mL SILICA DIMETHYL SILYLATE 15 [hp_X]/10mL ALLYLTHIOUREA 15 [hp_X]/10mL
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59262-275-11 Ear Ringing Remedy 10 mL in 1 BOTTLE, DROPPER SOLUTION 10 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59262-275 EAR RINGING REMEDY (ALLYLTHIOUREA, ARNICA MONTANA FLOWER, CALCIUM SULFIDE, ERIODICTYON CALIFORNICUM LEAF, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, QUININE SULFATE, SILICA DIMETHYL SILYLATE) SOLUTION [SIMILASAN CORPORATION] 3 Current NDC, Legacy NDC, 1 package rows 20230106_6451c91d-ea16-484a-be11-5311434ee8db.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59262-275-11 59262027511 10 mL in 1 BOTTLE, DROPPER (59262-275-11) 10 ml 2018-01-01 0000-00-00 No No Current