NDC | 59262-272-11 |
Set ID | 1b548338-f9f0-4a63-b553-df4fcd18d594 |
Category | HUMAN OTC DRUG LABEL |
Packager | Similasan Corporation |
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Product Class | |
Product Number | |
Application Number |
- Active Ingredient
- Purpose
- Active Ingredients
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
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Uses:
For occasional use as an aid to soften, loosen, and remove excess ear wax. According to homeopathic principles, the ingredients in this medication also provide temporary relief from symptoms such as:
- clogged sensation when caused by ear wax
- ringing in the ear when caused by ear wax
- dry skin and itching of the ear canal
- Warnings:
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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 3 days; if excessive ear wax remains after the use of this product, consult a doctor
- with ear tubes
- If pregnant or breast feeding,
- Keep out of reach of children.
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Directions:
FOR USE IN THE EAR ONLY.
For adults and children, over 12 years of age:
- remove tamper evident seal from neck of bottle
- twist cap off bottle
- tilt head sideways, squeeze plastic applicator to release 2-3 drops into ear. (Tip of applicator should not enter ear canal.)
- keep drops in ear for several minutes by keeping head tilted or placing cotton in ear
- use twice daily for up to 3 days if needed, or as directed by a doctor
- any wax remaining after treatment may be removed by gently flushing the ear with warm water, using a soft, rubber bulb ear syringe
- children under 12 years of age: consult a doctor
- Other information:
- Inactive ingredient:
- Questions?
- Principle Display Panel
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INGREDIENTS AND APPEARANCE
EAR WAX RELIEF
causticum, graphite, lachesis muta venom and lycopodium clavatum spore solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59262-272 Route of Administration AURICULAR (OTIC) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU) CAUSTICUM 12 [hp_X] in 10 mL GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 15 [hp_X] in 10 mL LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 12 [hp_X] in 10 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 12 [hp_X] in 10 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59262-272-11 10 mL in 1 BOTTLE, DROPPER; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 06/01/2003 Labeler - Similasan Corporation (111566530)