Cle De Peau Beaute Concealer N Stick
Product Images NDC 58411-658

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Cle De Peau Beaute Concealer N (NDC 58411-658). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Shiseido Americas Corporation, 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

Principal Display Panel (5 g Cartridge Carton)

Principal Display Panel (5 g Cartridge Carton)
This is a drug information sheet for a product that appears to be a sunscreen. The product contains both active and inactive ingredients that are not specified clearly. It warns that spending time in the sun may cause skin cancer and premature aging of the skin, and recommends wearing protective clothing and using a broad-spectrum sunscreen with an SPF of 5 or higher. The container should be protected from heat and direct sun, and must be kept out of reach of children. The product should be used externally only, and users should seek medical help in case of allergic reactions or other symptoms. Contact information for the manufacturer is provided.*
FDA Label Image

Principal Display Panel (5 g Cartridge Carton)

Principal Display Panel (5 g Cartridge Carton)
This is a drug label that provides information to consumers about the medication. It lists the inactive ingredients present in the drug and provides instructions regarding application, sun protection usage, warnings, and precautions. It also includes a warning to protect the drug from excessive heat and direct sun. The label recommends wearing long-sleeve shirts, pants, hats, and sunglasses when spending time in the sun, regularly using a sunscreen with a broad spectrum SPF of 15 or higher, and limiting time in the sun. The label also warns to keep the product out of reach of children and to consult a doctor if necessary. The label provides a phone number for any queries or comments.*
FDA Label Image

Principal Display Panel (5 g Cartridge Carton)

Principal Display Panel (5 g Cartridge Carton)
This is a drug information sheet that provides the user with instructions on how to use the product correctly to avoid skin cancer and early skin aging. It also lists the inactive ingredients used in manufacturing the drug and provides warnings and precautions about its use. In case of any inquiries, users can utilize a toll-free number provided.*
FDA Label Image

Principal Display Panel (5 g Cartridge Carton)

Principal Display Panel (5 g Cartridge Carton)
This appears to be a section of a document describing the inactive ingredients and instructions for use of a drug or sunscreen. The inactive ingredients include extracts and compounds such as aluminum ERYTHRITOL, diphenylsiloxylphenyl trimethicone, and various types of glycols. The product is labeled for external use only and includes warnings about sun exposure and protection measures. The provided product information number is 1-800-906-7503, and there is a lot number/identifier on the bottom of the page.*
FDA Label Image

Principal Display Panel (5 g Cartridge Carton)

Principal Display Panel (5 g Cartridge Carton)
This is a drug information sheet that provides details on the inactive ingredients, directions for use, sun protection measures, warnings, and other information about the product. The sheet recommends using a sunscreen with a Broad Spectrum SPF of 5 or higher for protection against skin cancer and early skin aging. The product is for external use only and should be stored in a cool place. The sheet also provides a helpline number for questions or comments.*
FDA Label Image

Principal Display Panel (5 g Cartridge Carton)

FDA Label Image

Principal Display Panel (5 g Cartridge Carton)

Principal Display Panel (5 g Cartridge Carton)
This is a drug label with information on inactive ingredients, directions, warnings, sun protection measures, and other information. The inactive ingredients include ANGEBER AROMATICUS EXTRACT, ALUMINUM HYDROXIDE, DIPROPYLENE GLYCOL, PEG-8, DROMETRIZOLE TRISILOXANE, and WATER. The directions on how to use the drug entail the wearer to take sun protection measures, limit time in the sun, and wear protective clothing. The container is intended for external use only and should be protected from excessive heat and direct sun. There is a contact number for questions or comments.*
FDA Label Image

Principal Display Panel (5 g Cartridge Carton)

Principal Display Panel (5 g Cartridge Carton)
The text seems to provide information regarding a drug and its inactive ingredients. It also mentions directions and warnings for the usage of a sunscreen that offers sun protection measures. The product is for external use only and must be kept away from children. The text also includes information on contacting customer support.*
FDA Label Image

Principal Display Panel (5 g Cartridge Carton)

FDA Label Image

Principal Display Panel (5 g Cartridge Carton)

Principal Display Panel (5 g Cartridge Carton)
This is a drug information leaflet. The leaflet lists the drug facts of the medication, the inactive ingredients, directions and warnings for use. It advises users to protect against sun rays to prevent skin cancer and aging, especially for children under six months, to use sunscreen with SPF of 5 or higher to decrease the risk of skin cancer, and to wear protective clothing. The user is also required to avoid the sun from 10 am to 2 pm. If the medication has negative effects on the user, they should stop taking it and speak to a doctor about it. The dosage of the medication for children under six months should be confirmed with a doctor. It also contains contact information to call if there are any further questions or comments on the medication. There is a list of inactive ingredients available, and the intended use of the drug is not specified.*
FDA Label Image

Principal Display Panel (5 g Cartridge Carton)

Principal Display Panel (5 g Cartridge Carton)
This is a drug facts label. It provides information about the inactive ingredients, directions, sun protection measures, warnings, and other information related to a product, but it does not specify the name of the product. The product contains a sunscreen with broad-spectrum SPF of 5 or higher and has instructions for external use only. It is supposed to be kept away from children and protected from excessive heat and direct sun. It also lists some inactive ingredients, including alumina, water, and various extracts. The label provides a toll-free number for questions or comments.*
FDA Label Image

Principal Display Panel (5 g Cartridge Carton)

Principal Display Panel (5 g Cartridge Carton)
This is a drug fact sheet for a sunscreen product. It mentions the active ingredients, the importance of using sun protection to reduce the risk of skin cancer and aging, and directions for use. The inactive ingredients have also been listed. There is a warning to keep the product out of reach of children and to seek medical help if needed. The text also provides a phone number for questions or comments.*

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