FDA recall record

Den-Mat Holdings OralProCare medicated lip treatment, Net Wt 9.9 g (0.35 oz) tube, Ethyl recall — FDA D-0286-2024

CGMP Deviations: products may not conform to the labeled specifications.

Class IIclassification
D-0286-2024official record ID
Feb 7, 2024report date

Recall record at a glance

Official recordD-0286-2024
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmDen-Mat Holdings, LLC
Report dateFeb 7, 2024
Recall initiation dateJan 16, 2024
Quantity344 tubes
LocationLompoc, CA, United States

Official product description

OralProCare medicated lip treatment, Net Wt 9.9 g (0.35 oz) tube, Ethyl alcohol 6.0% Antibacterial, Manufactured by: Den-Mat Holdings, LLC, Lompoc, CA, 93436, USA, NDC 59883-500-01, UPC: 3 59883 00000 4.

Why the product was recalled

CGMP Deviations: products may not conform to the labeled specifications.

Distribution information

Nationwide in the US

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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