Ozcare Antiseptic Hand Sanitizer
Product Images NDC 75584-001

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Ozcare Antiseptic Hand Sanitizer (NDC 75584-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Reed Holdings Australia, Pty. Ltd., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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FDA Label Image

Label (Label)

Label (Label)
This is a drug fact description of a sanitizer spray with ethyl alcohol 70% used for hand washing to reduce the presence of bacteria on the skin. It contains aloe vera extract, disodium EDTA, eucalyptus oil, glycerin, lavender oil, tocopherol acetate, and triethanolamine as inactive ingredients. It warns that the sanitizer is flammable and should be kept away from fire or flame, for external use only, should not be used in eyes, and should be kept out of reach of children. In case of irritation, redness, or if the symptom persists for more than 72 hours, users should contact a doctor or Poison Control Centre. The product is manufactured by Reed Holdings Australia Pty Ltd, Cranbourne West, Victoria, Australia. The expiry date is 04/04/2022, and it comes in 8.5 fl oz (250 ml) spray bottle.*

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