Inoculex Hand Sanitizer
FDA Label NDC 77017-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Private Label Supplements for the product Inoculex Hand Sanitizer (NDC 77017-015). 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 drug facts, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, storage and handling, 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 70%
Otc - Purpose
Purpose
Antiseptic
Indications & Usage
Use as hand sanitizer to help reduce bacteria on the skin
Warnings
Warnings
Flammable, keep away from fire or flame.
For external use only.
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or redness develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children if swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Directions • apply palmful to hands • rub hands together vigorously until dry • supervise children in the use of this product.
Storage And Handling
Other Information store below 110°F (43°C) • may discolor certain fabrics or surfaces.
Inactive Ingredient
Inactive ingredients: Fragrance, Glycerol, Hydrogen Peroxide, *Hydroxypropyl Cellulose, *Hydroxypropyl Methycellulose, Water
*May or may not include
Other
www.inoculex.com
Distributed by: Inoculex, LLC
16 S Pennsylvania Ave.,
Oklahoma City, OK 73107
Made in the USA
* Please review the disclaimer below.
