Minoxidil 7% / Tretinoin 0.025%
Product Images NDC 72934-4150

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Minoxidil 7% / Tretinoin 0.025% (NDC 72934-4150). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Ewe (8 End)

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.*

FDA Label Image

Ff (4150 8 Front)

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.*

FDA Label Image

Et (4150 8 Middle)

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).*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.