Unguentine Original Maximum Strength Pain recall: CGMP Deviations
Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Oxide 6.6%), packaged in 1 oz. (28.3g) metal tubes, Distributed by: Oakhurst Company Levittown, NY 11756
Why was Unguentine Original Maximum Strength Pain recalled?
CGMP DEVIATIONS
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 1E346A, Exp. Date Nov-23; 2E304A, Exp. Date Oct-24
- Product
- Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Oxide 6.6%), packaged in 1 oz. (28.3g) metal tubes, Distributed by: Oakhurst Company Levittown, NY 11756
- Recalling firm
- Ecometics, Inc.
- Distribution
- Nationwide within the United States
- Recall date
- March 15, 2023
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)