Home NDC 59262-272 Ear Wax Relief
Product NDC 59262-272
11-digit product format 592620272
Labeler code 59262
Product ID 59262-272_5851ed73-15f2-1925-e063-6294a90a96a8
Type HUMAN OTC DRUG
Nonproprietary name causticum, graphite, lachesis muta venom and lycopodium clavatum spore
Dosage form SOLUTION
Route AURICULAR (OTIC)
Labeler Similasan Corporation
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2003-06-01
Substance CAUSTICUM; GRAPHITE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE
Active strength 12; 15; 12; 12 [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL; [hp_X]/10mL
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 · 14 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 2025-04-01 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 59262-272-11 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 59262-272-11 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 59262-272-11 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 59262-272-11 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 59262-272-11 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 59262-272-11 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 59262-272-11 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 Wax Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAUSTICUM 12 [hp_X]/10mL GRAPHITE 15 [hp_X]/10mL LACHESIS MUTA VENOM 12 [hp_X]/10mL LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/10mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59262-272-11 Ear Wax Relief 10 mL in 1 BOTTLE, DROPPER SOLUTION 10 12
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CAUSTICUM ACTIVE INGREDIENT DD5FO1WKFU EAR WAX RELIEF (CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE) SOLUTION [SIMILASAN CORPORATION] 9 GRAPHITE ACTIVE INGREDIENT 4QQN74LH4O EAR WAX RELIEF (CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE) SOLUTION [SIMILASAN CORPORATION] 9 LACHESIS MUTA VENOM ACTIVE INGREDIENT VSW71SS07I EAR WAX RELIEF (CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE) SOLUTION [SIMILASAN CORPORATION] 9 LYCOPODIUM CLAVATUM SPORE ACTIVE INGREDIENT C88X29Y479 EAR WAX RELIEF (CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE) SOLUTION [SIMILASAN CORPORATION] 9 CAUSTICUM ACTIVE MOIETY DD5FO1WKFU EAR WAX RELIEF (CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE) SOLUTION [SIMILASAN CORPORATION] 9 GRAPHITE ACTIVE MOIETY 4QQN74LH4O EAR WAX RELIEF (CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE) SOLUTION [SIMILASAN CORPORATION] 9 LACHESIS MUTA VENOM ACTIVE MOIETY VSW71SS07I EAR WAX RELIEF (CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE) SOLUTION [SIMILASAN CORPORATION] 9 LYCOPODIUM CLAVATUM SPORE ACTIVE MOIETY C88X29Y479 EAR WAX RELIEF (CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE) SOLUTION [SIMILASAN CORPORATION] 9 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX EAR WAX RELIEF (CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE) SOLUTION [SIMILASAN CORPORATION] 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59262-272 EAR WAX RELIEF (CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE) SOLUTION [SIMILASAN CORPORATION] 12 Current NDC, Legacy NDC, 1 package rows 20250410_1b548338-f9f0-4a63-b553-df4fcd18d594.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ear Wax Relief CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE Similasan Corporation 1b548338-f9f0-4a63-b553-df4fcd18d594 2026-08-05 Warnings Exact identifier ndc (product): 59262-272
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59262-272-11 59262027211 10 mL in 1 BOTTLE, DROPPER (59262-272-11) 10 ml 2003-06-01 0000-00-00 No No Current