QUALITY CHOICE EARWAX REMOVAL DROPS- carbamide peroxide liquid 
Chain Drug Marketing Association, Inc.

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Quality Choice Earwax Removal Drops

Drug facts


Active ingredient

Carbamide peroxide 6.5%

Purpose

Earwax removal aid

Uses

for occasional use as an aid to soften, looser, and remove excessive earwax

Warnings

For use in the ear only

Ask a doctor before use if you have

  • Ear drainage or discharge
  • Ear pain
  • Irritation, or rash in the ear
  • Dizziness
  • An injury or perforation (hole) of the ear drum
  • Recently had ear surgery

When using this product

avoid contact with the eyes

Stop use and ask a doctor if

  • You need to use for more than 4 days
  • Excessive earwax remains after use of this product

Keep out of reach of children

If swallowed get medical help or contact a Poison Control Center right away.

Directions

FOR USE IN THE EAR ONLYAdults and children over 12 years of age:

Children under 12 years: consult a doctor

Other information

Inactive ingredients

anhydrous citric acid, glycerin, propylene glycol, sodium citrate, sodium lauryl sulfate, water

Questions?

1-800-328-5890

*This product is not manufactured or distributed by Prestige Brands Inc. owner of the registered trademark Debrox. Distributed by C.D.M.A., Inc.  43157 W. Nine Mile Novi, MI 48376-0995  www.qualitychoice.com  Questions: 248-449-9300

Quality Choice Earwax Removal Drops Earwax Removal Aid  Carbamide Peroxide 6.5%  Safe, Gentle, Non-Irritating   0.5 FL OZ (15mL)

Product Labels

image description

QUALITY CHOICE EARWAX REMOVAL DROPS 
carbamide peroxide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-027
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBAMIDE PEROXIDE (UNII: 31PZ2VAU81) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) CARBAMIDE PEROXIDE65 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-027-161 in 1 CARTON11/27/2014
115 mL in 1 BOTTLE, DISPENSING; Type 1: Convenience Kit of Co-Package
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01411/27/2014
Labeler - Chain Drug Marketing Association, Inc. (011920774)
Establishment
NameAddressID/FEIBusiness Operations
Bell Pharmaceuticals, Inc.140653770manufacture(63868-027)

Revised: 12/2023
Document Id: 0c868adb-99ab-5c7a-e063-6394a90a6638
Set id: d8fd8102-114f-415d-9083-f98a63f9d1b3
Version: 3
Effective Time: 20231215
 
Chain Drug Marketing Association, Inc.