EARWAX REMOVAL DROPS- carbamide peroxide 6.5% liquid 
Pharma Nobis, LLC

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Private Label Earwax Removal- 0097

Citric Acid

Flavor

Glycerin

Propylene Glycol

Sodium Lauroyl Sarcosinate

Sodium Stannate

Purified Water

Earwax removal aid.

Adults and children over 12 yrs of age: tilt head to the side and place 5 to 10 drops into the ear canal.

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

For External Use Only.

Ask a doctor before use if you have:

Ear drainage or discharge

Ear pain, irritation, or rash in the ear

Recently had ear surgery

Dizziness

An injury or perforation (hole) of the eadrum

Carbamide Peroxide 6.5%

For occasional use as an aid to soften, loosen and remove excessive earwax.

CVS Label

CVSWax.jpgcarton

Leader Label

Leader Earwax Carton 12-30-22Leader Earwax Label 12-30-22Leader2022LDREarwax45.jpgLDREwawax90.jpg

Rite Aid Label

Rite Aid Earwax Carton 12-30-22Rite Aid Earwax Label 12-30-22Rite Aid Earwax Kit 2022RAEarwax45.jpgRAEarwax90.jpg

Major Label

MajorEarwax90.jpg

EARWAX REMOVAL DROPS 
carbamide peroxide 6.5% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82645-910
Route of AdministrationAURICULAR (OTIC)
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBAMIDE PEROXIDE (UNII: 31PZ2VAU81) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) CARBAMIDE PEROXIDE0.065 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM STANNATE (UNII: NJ7C1V83KG)  
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82645-910-901 in 1 CARTON06/04/2019
115 mL in 1 CONTAINER; Type 0: Not a Combination Product
2NDC:82645-910-451 in 1 CARTON06/04/2019
215 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01406/04/2019
Labeler - Pharma Nobis, LLC (118564114)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114manufacture(82645-910) , analysis(82645-910) , pack(82645-910) , label(82645-910)

Revised: 12/2023
Document Id: 0d1cdfd7-c2cf-9fd5-e063-6394a90a8eda
Set id: e21e114c-99b6-861c-e053-2995a90aeac1
Version: 3
Effective Time: 20231222
 
Pharma Nobis, LLC