Class II ยท Moderate risk
Debrox
CGMP Deviations: products were stored outside the drug label specifications.
National Drug Code
Is NDC 63029-0321-01 recalled?
Debrox · 1 BOTTLE, DROPPER in 1 CARTON (63029-321-01) / 15 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
1 FDA recall names the code 63029-0321-01 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.
- Active ingredient
- Carbamide Peroxide
- Strength
- CARBAMIDE PEROXIDE 65 mg/mL
- Form
- Liquid · Auricular (otic)
- Labeler
- Medtech Products Inc.
- Type
- Human OTC Drug
- Product code
- 63029-0321
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
- 63029-0103 Little Remedies Gas Relief Drops 1
Free recall alerts
Know the day your medication is recalled
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