Kern Sani, Inc Hand Sanitizer - Ocean Breeze Gel
Product Images NDC 77804-006

6 FDA label images from Kern Sani, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Kern Sani, Inc Hand Sanitizer - Ocean Breeze Gel (NDC 77804-006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kern Sani, Inc., 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

006-02 8oz Ocnbrz Gel (006 02 8oz Ocnbrz Gel)

006-02 8oz Ocnbrz Gel (006 02 8oz Ocnbrz Gel)
Label for Kern Sani, Inc Hand Sanitizer - Ocean Breeze Gel, an 8 fl oz (236 mL) bottle. The product is a non-sterile solution with 70% alcohol antiseptic. The front features the brand name, product name, and scent, while the back includes drug facts, directions, inactive ingredients, manufacturer details, barcode, lot number, and expiration date.*
FDA Label Image

006-03 16oz Ocnbrz Gel (006 03 16oz Ocnbrz Gel)

006-03 16oz Ocnbrz Gel (006 03 16oz Ocnbrz Gel)
Kern Sani, Inc Hand Sanitizer - Ocean Breeze Gel is a non-sterile solution with 70% alcohol antiseptic strength. The label features the product name prominently with a blue shield logo, and states the volume as 16 FL OZ (473 mL). It includes Drug Facts with active ingredient, uses, warnings, directions, and other information. Manufactured and distributed by Kern Sani, Inc in Bakersfield, CA.*
FDA Label Image

006-04 32oz Ocnbrz Gel (006 04 32oz Ocnbrz Gel)

006-04 32oz Ocnbrz Gel (006 04 32oz Ocnbrz Gel)
Kern Sani, Inc Hand Sanitizer - Ocean Breeze Gel is a 32 fl oz (946 mL) bottle of alcohol antiseptic solution with 70% alcohol content. The label highlights it as a non-sterile solution with a premium hand sanitizer formula. The back panel shows Drug Facts including active ingredient, uses, warnings, directions, and storage information. The product is manufactured and distributed by Kern Sani, Inc.*
FDA Label Image

006-11 1gal Ocnbrz Gel (006 11 1gal Ocnbrz Gel)

006-11 1gal Ocnbrz Gel (006 11 1gal Ocnbrz Gel)
The image shows the label for Kern Sani, Inc Hand Sanitizer - Ocean Breeze Gel, a 1-gallon (3785 mL) bottle of alcohol antiseptic with 70% alcohol content. The label includes the brand name "Kern Sani," the product name "Ocean Breeze Gel," and states it is a non-sterile solution. The label also features a Drug Facts panel detailing active ingredient, uses, warnings, directions, and inactive ingredients. It is manufactured and distributed by Kern Sani, Inc. in Bakersfield, CA.*
FDA Label Image

006-12 5gal Ocnbrz Gel (006 12 5gal Ocnbrz Gel)

006-12 5gal Ocnbrz Gel (006 12 5gal Ocnbrz Gel)
Label for Kern Sani, Inc Hand Sanitizer - Ocean Breeze Gel, 70% alcohol antiseptic, 5 gallons (18925 mL). The label features the brand name KERN SANI with 'Premium Hand Sanitizer' and a shield emblem with leaves and water droplets. The label includes drug facts detailing active ingredient, uses, warnings, directions, and inactive ingredients. Manufactured and distributed by Kern Sani, Inc. in Bakersfield, CA.*
FDA Label Image

006-13 50gal Ocnbrz Gel (006 13 50gal Ocnbrz Gel)

006-13 50gal Ocnbrz Gel (006 13 50gal Ocnbrz Gel)
Kern Sani, Inc Hand Sanitizer - Ocean Breeze Gel label for a 50-gallon (189,250 mL) container. The label indicates the product is a non-sterile solution with 70% alcohol antiseptic. It includes usage, warnings, and directions, plus manufacturer information from Kern Sani, Inc in Bakersfield, CA. The label features the proprietary name and a blue and red color scheme.*

* 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.