Moistureworx
Product Images NDC 28109-020

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Moistureworx (NDC 28109-020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dermworx Incorporated, 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

Figure 1 (Trans-epidermal Water Loss Measurements)

A bar graph titled "TEWL Measurements (after 2 hours)" comparing the difference between treated and untreated skin sites. It shows two bars, one for MoistureWorx Spray Leave-on and one for MoistureWorx Spray Wipe-off, with both showing statistically significant differences (p<0.05). The graph quantifies skin water loss reduction for each product application type.*

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Figure 2 (Moisturization Study)

A bar chart titled 'Moisturization Study (NOVA Measurements)' comparing increased moisturization between treated and untreated sites over time. It shows percentage increases at 1-hour, 2-hour, 4-hour, and 6-hour intervals for MoistureWorx Spray Leave-on and Spray Wipe-off formulations, with statistical significance noted as p<0.05 for several comparisons.*

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Figure 3 (Barrier Durability)

A 3D bar graph titled 'Barrier Durability' comparing irritation levels over time (Hour 2, Hour 4, Hour 8) between untreated skin and skin treated with MoistureWorx Spray. The chart shows lower irritation for MoistureWorx Spray at each time point, with statistical significance (p<0.05) at Hour 4 and Hour 8. The irritant used is 12.5% Sodium Lauryl Sulfate.*

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Figure 4 (Barrier Durability)

A bar chart titled 'Barrier Durability' comparing irritation levels over time at Hour 2, Hour 4, and Hour 8. The chart compares untreated skin and skin treated with MoistureWorx™ Spray, showing lower irritation levels with the spray treatment, with data statistical significance indicated (p<0.05) at Hour 8. The irritant used is 0.75N Sodium Hydroxide.*

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Principal Display Panel (Bottle Label Front)

MoistureWorx Skin Protection Spray label showing 30% White Petrolatum, USP in a 4 fl. oz. (120 mL) bottle by DermWorx Incorporated. The label states the product is hypoallergenic, noncomedogenic, fragrance-free, and designed to gently cleanse and moisturize skin while delivering targeted white petrolatum.*

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Principal Display Panel (Bottle Label Back)

Drug Facts panel for MoistureWorx by DermWorx Incorporated lists active ingredient White Petrolatum USP 30% and inactive ingredients including cholesterol, diazolidinyl urea, glyceril distearate, methylparaben, and others. It describes skin benefits such as preventing chapped skin and effects of wind and cold weather. Directions recommend applying as needed with warnings for external use only and caution to avoid eyes. It provides usage restrictions, advice to consult a doctor if condition worsens, and includes safety information about keeping out of reach of children and when to seek medical help.*

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Principal Display Panel (Outer Carton Label)

MoistureWorx Skin Protection Spray packaging label displays 30% White Petrolatum, USP as the active ingredient. The label highlights a clinically proven, patented nanotechnology formula that moisturizes and protects the skin. It is marked as hypoallergenic, noncomedogenic, and fragrance-free. The unit contains six 4 fl oz (120 ml) bottles and is distributed by DermWorx Incorporated.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.