Naturally Nova Scotia Hand Sanitizer
FDA Label NDC 59958-100

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Owen Biosciences, Inc. for the product Naturally Nova Scotia Hand Sanitizer (NDC 59958-100). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, uses:, cautions and warnings:, directions:, inactive ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

ACTIVE INGREDIENT: Ethyl Alcohol* (Antiseptic) 62%

Uses:

To decrease bacteria on the skin that could cause disease.Recommended for repeated use.  Kills 99.9% of common harmfulgerms and bacteria within 30 seconds.

Cautions And Warnings:

For external use only. Flammable, keep away fromfire or flame.  Keep out of reach ofchildren.  Store at 20 to 25°C.  Maydiscolor some fabrics.

Directions:

Apply to hands and rub in thoroughly until dry.

Inactive Ingredients:

Water, Coco Glycerides*, Safflower FattyAcids*, Coconut Fatty Acids*, Glycerin*, Bentonite, Silicia, Vanilla*(Vanilla planifolia) Fruit Flavour, Peppermint* (Mentha piperita) Oil,Tocopherol (vitamin E), Potasium Hydroxide.*Certified organic

* Please review the disclaimer below.