Product Images Fluocinolone Acetonide 0.01% / Minoxidil 7% / Progesterone 0.1%
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Product Label Images
The following 3 images provide visual information about the product associated with Fluocinolone Acetonide 0.01% / Minoxidil 7% / Progesterone 0.1% NDC 72934-4080 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 for an external product. It instructs to apply topically and recommends storing at a controlled room temperature. The product is manufactured and distributed by Sincerus Florida, LLC in Pompano Beach, FL. It also provides contact information for reporting adverse reactions to the manufacturer or FDA. The product is not for resale.*
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This appears to be a product code for a medication containing an active ingredient called "LUOCINOLONE Ac:ETONID" at a strength of "USP0.0105" or "1%". There is also a reference to NDC (National Drug Code) which is a unique identifier for medications in the United States. The remaining text is not readable and appears to be a error.*
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This is a prescription medicine with fluocinolone acetonide USP and minoxidil USP as active ingredients. The manufacturing date is January 1, 1970, and the lot number is 031092ABCDEFGH@1. The medicine also contains Ethyl Alcohol USP, Lactic Acid USP, and Propylene Glycol USP as additional components.*
* 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.