Ear Wax Relief

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Ear Wax Relief
Generic name
CAUSTICUM, GRAPHITE, LACHESIS MUTA VENOM AND LYCOPODIUM CLAVATUM SPORE
Manufacturer
Similasan Corporation
Product type
HUMAN OTC DRUG
SPL set ID
1b548338-f9f0-4a63-b553-df4fcd18d594
SPL ID
5851ed73-15f2-1925-e063-6294a90a96a8
Version
13
Effective date
2026-08-05
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:48:38
Harmonized routes table
Harmonized routes
AURICULAR (OTIC)

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: According to homeopathic principles, symptoms may temporarily worsen before improving (initial exacerbation of symptoms). Avoid contact with eyes. If pregnant, trying to get pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Do not use: if you have ear drainage, discharge, ear pain, irritation, a rash in the ear, or are dizzy; consult a doctor if you have an injury or perforation (hole) of the ear drum or after ear surgery unless directed by a doctor for more than 48 hours; if excessive ear wax remains after the use of this product, consult a doctor with ear tubes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.