Pl Hand Sanitizer Wipe
Product Images NDC 80479-275

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Pl Hand Sanitizer Wipe (NDC 80479-275). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Newport Mfg 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

Ndc 80479-275-69 (Pl Hand Sanitizer Wipe)

Ndc 80479-275-69 (Pl Hand Sanitizer Wipe)
This text provides Drug Facts related to a sanitizer containing Ethyl Alcohol (75%) which is an antimicrobial agent. The product is recommended for repeated use to decrease bacteria on the skin. However, one must avoid contact with broken skin, eyes, or ingestion. The product must be kept away from fire and flames. It is recommended to stop using the product immediately if any irritation, redness develops, or the condition persists for more than 72 hours. It is advised to keep the product out of reach of children, and one should seek medical help or contact the Poison Control Center right away in case of ingestion. The product needs to be wet on hands thoroughly, and one needs to wait for it to dry without wiping. It is not recommended for use on infants, and adult supervision is necessary for children under 6. The product should be stored at 20-25° C (67-77° F), and inactive ingredients used are Aloe Barbadensis Leaf Extract, Citrus Limon Peel D-Limonene, Glycerin, Water, Tocopherol Acetate (Vitamin E).*

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