Hand Sanitizer
Product Images NDC 77143-002

Product Visual Gallery

This gallery contains 17 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 77143-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Naturatlali S De Rl De Cv, 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

Gal Quarter (1 Gal (1))

Drug Facts label of Hand Sanitizer by NATURATLALI S DE RL DE CV, including active ingredient benzalkonium chloride 0.13% with antimicrobial purpose. The label provides uses, warnings, directions, and lists inactive ingredients in both English and Spanish.*

FDA Label Image

100 mL Quater Usa

The image contains the Drug Facts panel for Hand Sanitizer Gel by NATURATLALI S DE RL DE CV. It includes active ingredient benzalkonium chloride 0.13%, usage instructions, warnings, directions, and inactive ingredients. The label is bilingual in English and Spanish and also shows contact and manufacturing information, a barcode, and promotional claims about effectiveness against viruses and bacteria.*

FDA Label Image

1lquarter (1l)

Drug Facts panel of Hand Sanitizer by NATURATLALI S DE RL DE CV includes active ingredient benzalkonium chloride 0.13% as antimicrobial. It provides bilingual information in English and Spanish on use, warnings, directions, and inactive ingredients. Warnings cover external use only, flammability, and first aid measures. Directions advise applying product to hands and supervising young children. Inactive ingredients include water, alcohols, glycerin, parabens, and colorants.*

FDA Label Image

Quarter 250 (250 mL)

Label of Hand Sanitizer Gel by NATURATLALI S DE RL DE CV, containing 250 mL. The label features the brand name QUATER and specifies it as a hand sanitizer gel. The product includes drug facts information in English and Spanish, listing benzalkonium chloride 0.13% as the active ingredient with antimicrobial purpose. It also includes usage instructions, warnings, directions, and inactive ingredients.*

FDA Label Image

6. 77143 002 02

Label for NATURATLALI Alcohol-Free Hand Sanitizer Lotion with refreshing moisturizers and fresh clean scent. The product size is 16.6 fl oz (500 ml). The label indicates it is antimicrobial containing benzalkonium chloride 0.13% as the active ingredient, manufactured by NATURATLALI S DE RL DE CV in Mexico.*

FDA Label Image

7. 77143 002 03

Label for NATURATLALI Hand Sanitizer Alcohol-Free Lotion with refreshing moisturizers and fresh clean scent. The product volume is 8.3 FL OZ (250 ML). The Drug Facts panel highlights benzalkonium chloride 0.13% as the active ingredient with antimicrobial purpose and includes warnings, directions, and inactive ingredients. Manufactured by NATURATLALI S DE RL DE CV in Mexico.*

FDA Label Image

8. 77143 002 17

Label of NATURATLALI Hand Sanitizer Alcohol-Free Lotion, 1 gallon (3.785 L) size. The product is an alcohol-free hand sanitizer lotion with refreshing moisturizers and fresh clean scent. The label includes the NATURATLALI logo and highlights features such as effectiveness against harmful germs and nourishing moisturizers. Manufactured by NATURATLALI S DE RL DE CV, the label also displays a barcode and some drug facts information.*

FDA Label Image

Cp Gal (Crown Packaging 1gal)

Drug Facts label for Hand Sanitizer Gel by NATURATLALI S DE RL DE CV. The label shows active ingredient Benzalkonium chloride 0.13%, with information on uses, warnings, directions, and inactive ingredients in English and Spanish. The content includes antimicrobial purpose, instructions for use, cautions about flammability and contact with eyes, and supervision of children under 6.*

FDA Label Image

Cp 1l (Crown Packaging 1l)

Drug Facts panel for Hand Sanitizer Gel by Crown Packaging Corp. in English and Spanish. It includes the active ingredient benzalkonium chloride 0.13% as antimicrobial, uses to reduce bacteria, warnings about flammability and eye contact, directions for application, and a list of inactive ingredients such as water, isopropyl alcohol, glycerin, and preservatives.*

FDA Label Image

Cp 500ml (Crown Packaging 500ml)

Hand Sanitizer Gel, 16.6 FL OZ (500 mL) packaged by Crown Packaging Corp. The label includes bilingual English and Spanish text. The product's active ingredient is benzalkonium chloride 0.13%, listed as antimicrobial. The label provides warnings, usage instructions, inactive ingredients, and manufacturer details from Crown Packaging Corporation in Chesterfield, MO, USA.*

FDA Label Image

Alpha 1l (Etiqueta Alpha Gel 1l Fda)

Label for Alpha-Gel Hand Sanitizer in a 33.8 fl oz (1 quart) bottle. The active ingredient is benzalkonium chloride 0.13%. The label includes bilingual drug facts with usage instructions, warnings, inactive ingredients, and contact email. The product is manufactured by NATURATLALI S DE RL DE CV and displays a barcode and NDC 77143-003-06.*

FDA Label Image

Alpha 250 (Etiqueta Alpha Gel 250ml Fda)

Drug Facts panel for Hand Sanitizer by NATURATLALI S DE RL DE CV includes active ingredient benzalkonium chloride 0.13% as an antimicrobial. It provides usage instructions, warnings, directions for application, inactive ingredients, and safety measures in both English and Spanish. The 250 mL product label also features a barcode and manufacturer contact email.*

FDA Label Image

Alpha 500ml (Etiqueta Alpha Gel 500ml Fda)

Drug Facts label for Hand Sanitizer by NATURATLALI S DE RL DE CV, containing active ingredient benzalkonium chloride 0.13%. The label provides usage instructions, warnings, and directions for application to hands. It includes inactive ingredients, safety information about avoiding contact with eyes, supervision of children, and disposal warnings. The label is bilingual in English and Spanish, with a volume indication of 500 mL seen on a separate part of the packaging.*

FDA Label Image

Alpha 5l (Etiqueta Alpha Gel 5l Fda)

Drug Facts panel for Hand Sanitizer by NATURATLALI S DE RL DE CV includes active ingredient benzalkonium chloride 0.13% with antimicrobial purpose. The label provides uses, warnings, directions, inactive ingredients, and contact information for questions. It is bilingual, in English and Spanish, and specifies a 5000 mL volume.*

FDA Label Image

5 L (Nat500l)

Drug Facts panel for Hand Sanitizer by NATURATLALI S DE RL DE CV includes active ingredient benzalkonium chloride 0.13% as an antimicrobial. It details uses, warnings, directions for use, and inactive ingredients such as water, glycerin, and propylene glycol. Instructions on application and precautions like avoiding contact with eyes and keeping out of children’s reach are provided in English and Spanish.*

FDA Label Image

Quarter 500 (Q500ml)

Drug Facts panel from Hand Sanitizer Gel by NATURATLALI S DE RL DE CV, showing active ingredient benzalkonium chloride 0.13% with antimicrobial purpose. Includes bilingual English-Spanish sections for use, warnings, directions, and inactive ingredients. Instructions emphasize external use only, flammability, precautions to keep out of eyes and children, and directions for application and supervision of young children.*

FDA Label Image

Q5l (Q5l)

Drug Facts panel for Hand Sanitizer Gel by NATURATLALI S DE RL DE CV in both English and Spanish. It lists benzalkonium chloride 0.13% as the active antimicrobial ingredient, usage instructions, warnings including flammability and external use only, directions for use, and inactive ingredients such as water, alcohols, parabens, and color additives. The text covers safety and application guidance bilingually.*

* 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.