Class II · Moderate risk
CAREone
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
National Drug Code
Is NDC 72476-0838-34 recalled?
CareOne Earwax Removal Drops · 1 BOTTLE in 1 BOX (72476-838-34) / 15 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 72476-0838-34 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
- Retail Business Services, LLC
- Type
- Human OTC Drug
- Product code
- 72476-0838
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
- 72476-0127 Extra Strength Antacid 1
- 72476-0178 Ultra Strength Antacid Assorted Berries 1
- 72476-0847 careone allergy relief 1
Free recall alerts
Know the day your medication is recalled
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