Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule recall
Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle, This is a compounded drug not for resale, Store at room temperature…
Why was Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule recalled?
Super-potent Drug: This recall has been initiated due to the elevated presence of minoxidil and biotin.
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 #: 01-09-2020:13@8, Exp. 7/7/2020
- Product
- Minoxidil/Biotin/Spironolactone 1.25/5/25 mg capsule, 90 capsules per bottle, This is a compounded drug not for resale, Store at room temperature…
- Recalling firm
- MasterPharm LLC
- Quantity
- 300 capsules
- Distribution
- FL and MD
- Recall date
- July 8, 2020
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)