Extreme Sanitizer
Product Images NDC 77868-0001

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Extreme Sanitizer (NDC 77868-0001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Earth Wind Fire L.l.c. / Extreme Sanitizer�, 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 Ingredient (Activeingredient)

A Drug Facts panel listing Alkylbenzyldimethylammonium Chloride (Quaternary Ammonium) at 0.13% as the active ingredient classified as an antiseptic.*

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Dosage And Admin (Dosage And Admin)

Partial drug facts panel for Extreme Sanitizer showing active ingredient Alkylbenzyldimethylammonium Chloride 0.13%. Includes use instructions for hand sanitation without water wash, warnings about eye contact and irritation, and directions to apply spray fully to hands with repeated application increasing effect.*

FDA Label Image

Extreme Sanitizer® (Extremesanitizer)

The label for Extreme Sanitizer by Earth Wind Fire L.L.C. displays the brand name prominently with claims of killing 99.99% of germs in 15 seconds and being effective, hypoallergenic, and alcohol-free. The product is an advanced formula hand sanitizer in a 2 FL OZ (60 mL) bottle, made in the USA. The label includes drug facts, active ingredient Alkylbenzyldimethylammonium Chloride 0.13%, directions for use, warnings, and storage information at 56-86 °F. Contact info and website are provided, along with a barcode and QR code.*

FDA Label Image

Use (Purpose)

A drug facts panel excerpt showing the active ingredient Alkylbenzyldimethylammonium Chloride (Quaternary Ammonium) 0.13%, labeled as an antiseptic. It includes use instructions stating the product is for hand sanitation and does not require water washing.*

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Questions (Questions)

A text panel listing an inactive ingredient as Water. It provides a contact email for questions: [email protected]. Additional storage information advises storing the product at 56 to 86 degrees Fahrenheit.*

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Do Not Use (Donotuse)

A warning and precaution text panel for Extreme Sanitizer. It advises to avoid eye contact and flush with water if exposed, keep out of reach of children, stop use if redness or irritation occurs, and call poison control if swallowed.*

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Inactive Ingredient (Inactive)

A partial view of a product label text panel showing the inactive ingredient section, listing Water as the inactive ingredient. The surrounding text is mostly obscured or cut off and not fully legible.*

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No Children (Nochildren)

A warning label panel for Extreme Sanitizer advising to avoid eye contact and flush with water if contacted, keep out of reach of children, stop use if redness or irritation occurs, and to call poison control if swallowed.*

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Other Info (Otherinfo)

A text snippet providing contact information for questions via an email address at extremesanitizer.com and a storage instruction to keep the product between 56 and 86 degrees Fahrenheit.*

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Waring (Stopuse)

A warning label section from the Extreme Sanitizer product, advising to avoid eye contact and flush with water, keep out of reach of children, stop use if redness or irritation occurs, and to call poison control if swallowed.*

FDA Label Image

Warning (Warning)

A warning and precaution text panel from Extreme Sanitizer by Earth Wind Fire L.L.C. It advises avoiding eye contact and flushing with water if contact occurs, keeping out of reach of children, stopping use if redness or irritation happens, and calling poison control if swallowed.*

* 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.