Product Images Minoxidil 7% / Tretinoin 0.025%
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Product Label Images
The following 3 images provide visual information about the product associated with Minoxidil 7% / Tretinoin 0.025% NDC 72934-4150 by Sincerus Florida, Llc, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.
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This text provides directions for use of a product; it advises that the item is only for external use, and to wash hands after use. The product should be stored at a controlled room temperature. The contact information for Sincerus Florida LLC is also provided, along with how to report suspected adverse reactions. It is noted that the item is not for resale and for office use only.*
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This is a product label for a solution containing 7% minoxidil and 0.025% tretinoin. The volume of the solution is 60gm and it has an NDC code of 72934-4150-8. The purpose or use case of the solution is not provided.*
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This text appears to be a prescription drug label. The lot number is 031081ABCDEFGH@1 and has a "Rx only" label, indicating it's only for prescription use. It also displays the date of manufacture (MFG) and the corresponding date for when the drug is no longer usable (BUD). The active ingredients include MIOAAINISE and the drug formulation is likely a liquid ("Ethyl Alcohol USP"), whereas, the 'Inactive Ingredient' list includes Butylated Hydroxytoluene NF (BHE).*
* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.