Tri-luma Cream
Product Images NDC 0299-5950

4 FDA label images from Galderma Laboratories, L.p. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tri-luma (NDC 0299-5950). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Galderma Laboratories, L.p., 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

Fluocinolone-mol (Tri Figure 04)

Fluocinolone-mol (Tri Figure 04)
Chemical structure of fluocinolone acetonide, one of the active ingredients in TRI-LUMA topical cream. The diagram depicts the molecular arrangement including rings, bonds, and functional groups characteristic of fluocinolone acetonide.*
FDA Label Image

Hydro-mol (Tri Figure 02)

Hydro-mol (Tri Figure 02)
Chemical structure of hydroquinone, an active ingredient in TRI-LUMA topical cream containing fluocinolone acetonide, hydroquinone, and tretinoin.*
FDA Label Image

Tretinoin (Tri Figure 03)

Tretinoin (Tri Figure 03)
Chemical structure diagram of tretinoin, one of the active ingredients in TRI-LUMA cream, showing carbon, hydrogen, and oxygen atoms arranged in a polyene carboxylic acid configuration.*
FDA Label Image

30g-carton (P51399 6 Tri Luma 30 G Carton)

30g-carton (P51399 6 Tri Luma 30 G Carton)
TRI-LUMA cream containing fluocinolone acetonide 0.01%, hydroquinone 4%, and tretinoin 0.05% in a 30 g tube. Label indicates topical use only, with storage instructions to refrigerate at 2° to 8°C (36° to 46°F) and protect from freezing. Marketed by Galderma Laboratories, L.P., Dallas, TX. The packaging features dosage, ingredient details, NDC 0299-5950-30, and prescription only status.*

* 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.