Sanispire Hand Sanitizer
Product Images NDC 60717-811

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Sanispire Hand Sanitizer (NDC 60717-811). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rna Pharma, 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

Active Ingredients (Sani 32oz Active)

Drug Facts panel on a Sanispire Hand Sanitizer bottle showing active ingredient Ethyl Alcohol 70% v/v labeled as an antiseptic. The panel includes usage instructions for sanitizing hands, warnings about flammability and proper use, directions for application, and a list of inactive ingredients such as Acrylates, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Glycerin, Fragrance, and Water. The text emphasizes external use only and safety precautions.*

FDA Label Image

Dosage & Administration (Sani 32oz Directions)

Sanispire Hand Sanitizer in a clear plastic pump bottle showing a black pump dispenser. The label displays drug facts including the active ingredient ethyl alcohol 70% v/v and usage warnings. Labeler is RNA PHARMA, LLC. The bottle contains clear gel with visible bubbles inside.*

FDA Label Image

Inactive Ingredients (Sani 32oz Inactive)

Sanispire Hand Sanitizer in a clear plastic bottle with a black pump dispenser. The label displays the Drug Facts panel, revealing the active ingredient as Ethyl Alcohol 70% v/v, with antiseptic purpose. The bottle is filled with a clear gel containing suspended bubbles. The label also includes warnings, directions, and inactive ingredients. The product is labeled by RNA PHARMA, LLC.*

FDA Label Image

Keep Out Of Reach Of Children (Sani 32oz Keep Ou)

Drug Facts panel on Sanispire Hand Sanitizer showing active ingredient as Ethyl Alcohol 70% v/v with antiseptic purpose. The label provides usage instructions, warnings about flammability and external use only, precautions for children and wound use, directions for application, storage advice, and a list of inactive ingredients including acrylates and aloe leaf juice.*

FDA Label Image

Package Label Principal (Sani 32oz Principal)

Sanispire Hand Sanitizer moisturizing gel in a clear plastic pump bottle. The label highlights 70% ethyl alcohol as the active ingredient and a fresh lemon scent. The product is marked as made in the USA and made in an FDA-registered facility. The bottle size is 32 fl oz (940 ml).*

FDA Label Image

Purpose (Sani 32oz Purpose)

Sanispire Hand Sanitizer in a clear plastic bottle with a black pump. The bottle is filled with clear gel containing visible bubbles. A label on the back displays detailed drug facts including the active ingredient Ethyl Alcohol 70% v/v, warnings, directions, and inactive ingredients. The product is labeled by RNA PHARMA, LLC.*

FDA Label Image

Indications & Usage (Sani 32oz Use)

Sanispire Hand Sanitizer in a clear plastic pump bottle showing drug facts label prominently. The active ingredient listed is Ethyl Alcohol 70% v/v as antiseptic. The label includes usage instructions, warnings, and a list of inactive ingredients. The bottle contains a clear gel with visible air bubbles. The labeler is RNA PHARMA, LLC.*

FDA Label Image

Warnings (Sani 32oz Warnings)

Text panel showing the drug facts for Sanispire Hand Sanitizer. It lists ethyl alcohol 70% v/v as the active ingredient with the purpose of antiseptic. The panel includes sections on uses, warnings, directions, and other information, such as flammability and external use instructions. It also contains an inactive ingredients list and a barcode at the bottom.*

* 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.