Label: RITE AID EARWAX REMOVAL DROPS- carbamide peroxide liquid
- NDC Code(s): 11822-6117-0, 11822-6117-1
- Packager: Rite Aid
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 10, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Do not use
- if you have ear drainage or discharge, ear pain, irritation or rash in the ear, or are dizzy; consult a doctor
- if you have an injury or perforation (hole) of the eardrum or after ear surgery unless directed by a doctor
- for more than 4 days; if excessive earwax remains after use of this product, consult a doctor
When using this product avoid contact with the eyes. If accidental contact with the eyes occurs, flush your eyes with water and consult a doctor.
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
FOR IN EAR USE 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 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.
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RITE AID EARWAX REMOVAL DROPS
carbamide peroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-6117 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARBAMIDE PEROXIDE (UNII: 31PZ2VAU81) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) CARBAMIDE PEROXIDE 6.5 g in 100 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TARTARIC ACID (UNII: W4888I119H) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-6117-0 1 in 1 CARTON 05/10/2024 1 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:11822-6117-1 1 in 1 CARTON 05/10/2024 2 15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M014 05/10/2024 Labeler - Rite Aid (014578892) Registrant - Derma Care Research Labs, LLC (116817470) Establishment Name Address ID/FEI Business Operations Derma Care Research Labs, LLC 116817470 manufacture(11822-6117)
