Active Ingredient Purpose
Carbamide peroxide 6.5% Earwax removal aid
Earwax Removal Drops
FDA Label NDC 49035-537
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Walmart for the product Earwax Removal Drops (NDC 49035-537). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient purpose, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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 ear drum or after ear surgery, unless
directed by a doctor • for more than 4 consecutive
days; if excessive earwax remains after use of this
product, consult a doctor
* Please review the disclaimer below.
