Fluocinolone Acetonide 0.01% / Minoxidil 7% / Progesterone 0.1%
FDA Label NDC 72934-4080

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sincerus Florida, Llc for the product Fluocinolone Acetonide 0.01% / Minoxidil 7% / Progesterone 0.1% (NDC 72934-4080). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding directions for use, sincerus florida, llc. adverse reactions, active, inactive, ndc 72934-4080-8. fluocinolone acetonide usp 0.01% / minoxidil usp 7% / progesterone usp 0.1%. solution 60 gm., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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