Hand Sanitizer
Product Images NDC 77160-306

7 FDA label images from Karsof Systems Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 77160-306). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Karsof Systems 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

3785.41ml Ndc 77160-306-01 (01 Fda Gallon Gel Unscented)

3785.41ml Ndc 77160-306-01 (01   Fda Gallon Gel Unscented)
Label for Dr GermCleaner Hand Sanitizer Gel containing 80% Isopropyl Alcohol as the active ingredient. The product is unscented, in a 1 gallon (3.78 L) size, and identified with NDC 77160-306-01. Labeler is Ascend Herbs and the product is made in the USA. Includes Drug Facts with usage, warnings, directions, and inactive ingredients listed on the right side.*
FDA Label Image

946.353ml Ndc 77160-306-02 (02 Fda 32oz Gel Unscented)

946.353ml Ndc 77160-306-02 (02   Fda 32oz Gel Unscented)
Dr GermCleaner Isopropyl Alcohol Antiseptic 80% Topical Gel Hand Sanitizer by KARSOF SYSTEMS LLC. The label shows the product name, active ingredient concentration (80% isopropyl alcohol), gel form, unscented, and volume of 32 fluid ounces (946.353 ml). It includes branding from Ascend Herbs and indicates Made in USA with a barcode.*
FDA Label Image

473.176ml Ndc 77160-306-03 (03 Fda 16oz Gel Unscented)

473.176ml Ndc 77160-306-03 (03   Fda 16oz Gel Unscented)
Label for Dr GermCleaner Hand Sanitizer, an 80% isopropyl alcohol topical gel. The label shows the product is a 16 FL. OZ. (473 ml) unscented gel by Ascend Herbs, made in USA. It includes Drug Facts highlighting its antiseptic use and warnings, directions, and ingredients such as carbomer, glycerin, hydrogen peroxide, purified water USP, and aloe vera.*
FDA Label Image

236.588ml Ndc 77160-306-05 (04 Fda 8oz Gel Bottle Unscented)

236.588ml Ndc 77160-306-05 (04   Fda 8oz Gel Bottle Unscented)
Label for Dr GermCleaner Hand Sanitizer gel containing 80% isopropyl alcohol as antiseptic. The unscented topical gel is in an 8 fl oz (236.59 ml) container. The label features Ascend Herbs branding, is marked Made in USA, and includes usage warnings, directions, and inactive ingredients.*
FDA Label Image

118.294ml Ndc 77160-306-06 (05 Fda 4oz Gel Bottle Unscented)

118.294ml Ndc 77160-306-06 (05   Fda 4oz Gel Bottle Unscented)
Drug Facts panel for Hand Sanitizer with 80% Isopropyl Alcohol as active ingredient. Includes use instructions, warnings about flammability and unsafe usage, directions for application, storage information, and a list of inactive ingredients such as glycerin, hydrogen peroxide, and aloe vera.*
FDA Label Image

59.1471ml Ndc 77160-306-07 (06 Fda 2oz Gel Bottle Unscented)

59.1471ml Ndc 77160-306-07 (06   Fda 2oz Gel Bottle Unscented)
Dr GermCleaner Hand Sanitizer is a topical gel containing 80% isopropyl alcohol as an antiseptic. The unscented 2 fl oz gel is labeled by KARSOF SYSTEMS LLC and made in the USA. The label includes active and inactive ingredients, usage directions, warnings, and storage instructions.*
FDA Label Image

59.1471ml Ndc 77160-306-08 (07 Fda Keychain Gel Bottle Unscented)

59.1471ml Ndc 77160-306-08 (07   Fda Keychain Gel Bottle Unscented)
Dr Germ Cleaner Isopropyl Alcohol Antiseptic 80% Hand Sanitizer topical gel, 2 fl oz. The label shows the product name, strength, dosage form as gel, and notes it is unscented. Manufacturer information includes Ascend Herbs and KARSOF SYSTEMS LLC. The label also states it is made in the USA and includes a website URL. The NDC 77160-306-08 is printed vertically on the label.*

* 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.