Imiquimod 5% / Levocetirizine Dihydrochloride 1% / Tretinoin 0.05%
Product Images NDC 72934-1126

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Imiquimod 5% / Levocetirizine Dihydrochloride 1% / Tretinoin 0.05% (NDC 72934-1126). 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

X (1126 2 End)

This is a set of directions for use for an external use-only medication. It is advised to apply it topically and wash hands after use. It should be stored at controlled room temperature. The medication is produced by Sincerus Florida, LLC, and any suspected adverse reactions should be reported to them or to the FDA. It is not for resale and for office use only.*

FDA Label Image

X (1126 2 Front)

This appears to be a label for a medication with the brand name X'M. The label includes information on its ingredients and dosage: - NDC (National Drug Code) number: 72934-1126-2 - Active ingredients: Miquimod USP 5%, Evocetirizine Dihydrochloride USP 1%, Tretinoin USP 0.05% - Form: Gel - Size: 30g Without additional context or information, it's not possible to determine the specific use or indications for this medication.*

FDA Label Image

D (1126 2 Middle)

This appears to be a partial record of the active and inactive ingredients of a medication, but without additional context or information it is not possible to determine what the medication is for or how it should be used.*

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