Class II · Moderate risk
Audiologist's Choice
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
National Drug Code
Is NDC 59256-0836-34 recalled?
Audiologists Choice Earwax Removal Aid Drops · 1 BOTTLE, DISPENSING in 1 CARTON (59256-836-34) / 15 mL in 1 BOTTLE, DISPENSING
Yes — this exact package was recalled
1 FDA recall names the code 59256-0836-34 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Carbamide Peroxide
- Strength
- CARBAMIDE PEROXIDE 65 mg/mL
- Form
- Solution/ Drops · Auricular (otic)
- Labeler
- Oaktree Products Inc
- Type
- Human OTC Drug
- Product code
- 59256-0836
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 59256-0001 Audiologists Choice Earwax Removal System 1
Free recall alerts
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