Guard Gel
Product Images NDC 63148-455

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Guard (NDC 63148-455). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apollo Health And Beauty Care, 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

3 (06 27501 02 3 Oz)

Guard Advanced Hand Sanitizer gel with alcohol 70% antiseptic strength, contains aloe and vitamin E. The product volume is 3 FL OZ (89 mL). Manufactured and distributed by Apollo Health and Beauty Care in Canada, the label highlights antibacterial effectiveness and instructions for topical use to reduce bacteria on skin.*

FDA Label Image

32 (06 27505 06 32 Oz Frt)

Label of Guard Advanced Hand Sanitizer gel, 32 fl oz (946 mL), containing 70% ethyl alcohol. The front label highlights aloe and vitamin E ingredients and germ-killing efficacy. The back label presents Drug Facts, including active ingredient, warnings for external use and flammability, directions, inactive ingredients, and manufacturer details from Apollo Health and Beauty Care, Toronto, Canada.*

FDA Label Image

12 (06 27503 04 12 Oz)

Guard Advanced Hand Sanitizer gel with Aloe and Vitamin E, 12 FL OZ (355 mL) bottle. Contains 70% Ethyl Alcohol as an antiseptic. Manufactured and distributed by Apollo Health and Beauty Care, Toronto, Canada. Label highlights killing 99.99% of germs and bacteria on skin.*

FDA Label Image

6 (06 27507 08 60 Oz Frt)

Label for Guard Advanced Hand Sanitizer gel, topical use, containing 70 mL of alcohol per 100 mL. The front label highlights killing 99.99% of germs and includes Aloe and Vitamin E. The back label provides detailed Drug Facts, including active ingredient Ethyl Alcohol 70% as antiseptic, warnings, directions, inactive ingredients, manufacturer Apollo Health and Beauty Care, and recycling information. The product NDC is 63148-455-60.*

* 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.