Label: EAR WAX REMOVAL DROPS- carbamide peroxide - 6.5% solution/ drops
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated August 25, 2021
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- Active ingredient
- Stop Use and ask a Doctor if
- When using this product
- Keep out of the reach of children
Directions FOR USE IN THE EAR ONLY
- Adults and children over 12 years of age:
- Tilt head sideways and place 5 to 10 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 the ear.
- Use twice daily for up to 4 days if needed, or as directed by a doctor.
- Any earwax remaining after treatment may be removed by gently flushing the ear with warm water, using a soft rubber bulb ear syringe.
- When the ear canal is irrigated, the tip of the ear syringe should not obstruct the flow of water leaving the ear canal.
- Children under 12 years: consult a doctor.
- Other information
- Inactive ingredients
- Principal Display Panel Bottle Label 0.5 FL OZ
- Principal Display Panel - Carton label 0.5 FL OZ
- Principal Display Panel - Carton label KIT 0.5 FL OZ
INGREDIENTS AND APPEARANCE
EAR WAX REMOVAL DROPS
carbamide peroxide - 6.5% solution/ drops
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50804-341 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARBAMIDE PEROXIDE (UNII: 31PZ2VAU81) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) CARBAMIDE PEROXIDE 65 mg in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM CITRATE (UNII: 1Q73Q2JULR) SODIUM LAURYL SULFATE (UNII: 368GB5141J) TARTARIC ACID (UNII: W4888I119H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50804-341-51 1 in 1 CARTON 06/05/2019 1 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 2 NDC:50804-341-61 1 in 1 KIT 06/05/2019 2 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part344 06/05/2019 Labeler - GOODSENSE (076059836)