Sanitizer Solution, Formulation One
Product Images NDC 74401-700

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Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Sanitizer Solution, Formulation One (NDC 74401-700). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Volu-sol, 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

74401 700 02

74401 700 02
This is a drug facts label for a non-sterile solution of hand sanitizer containing 80% ethyl alcohol as the active ingredient. The solution is intended for use as a hand rub by healthcare personnel to reduce bacteria that can cause disease. The label provides warnings and directions for use, cautioning against use in children less than 2 months old and on open skin wounds, and advising users to keep the solution away from their eyes and out of reach of children. It also provides information on the manufacturer and the inactive ingredients in the product.*
FDA Label Image

74401 700 04

74401 700 04
This is a description of a Formula One Topical Solution for use as a Sanitizer Solution. The solution is a Non-sterile Solution that contains 80% Alcohol Antiseptic. The product code is WHO-004 NOC74401:700-04 and the container size is 120ml. However, the rest of the text is not readable.*
FDA Label Image

473 mL Label (74401 700 16 2)

473 mL Label (74401 700 16 2)
Sanitizer Solution is an alcohol antiseptic with 80% concentration. The formulation is a topical solution that is not for internal use. The product's DWHO016P NDC is 740170016. The date on the label is March 17th, 2020.*
FDA Label Image

1022 L Label (74401 700 27)

1022 L Label (74401 700 27)
V&LU-SO is a sanitizer solution, with 80% alcohol antiseptic, in a non-sterile topical solution formulation (Formulation One). Its NDC number is 74401-700-27 and has the WHO-270 reference. It is advised to keep away from flames, heat sources, sparks, and static discharge. For further information, refer to S505.*
FDA Label Image

946 mL Label (74401 700 32)

946 mL Label (74401 700 32)
This is a description of a sanitizer solution that is an alcohol antiseptic of 80% strength. It is a topical solution, nonsterile in nature and comes in a 946 mL/32 floz bottle. The formulation is identified by WHO-032PE and NDC code 74401-700-32. The solution is ideal for use as an antiseptic hand rub but caution must be taken to keep it away from flames, heat, sparks, and sources of static discharge. There is additional information available on S 505.*
FDA Label Image

74401 700 47

74401 700 47
This appears to be a label or description for a bottle of hand sanitizer solution. The solution is made from 80% alcohol and is likely meant to be used as an antiseptic to kill germs and bacteria on hands or surfaces. The text also mentions "WEMEN OWNED", suggesting that the company creating this product is owned and operated by women.*
FDA Label Image

208 L Label (74401 700 55)

208 L Label (74401 700 55)
This is a description of a sanitizer solution that contains 80% alcohol and is nonsterile. It comes in a 208L/55 gal container and is formulated as a topical solution. The product is identified with the code WHO-055 and NDC number 74401-700-55. The solution should be kept away from flames and discharged properly. It is an antiseptic hand rub. For further information, refer to section S 505.*

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