Otc - Active Ingredient
This product is owned as a deodorant active ingredients triclosan and aluminum chlorhydroxide. Mixed effect that produced is deodorant and antiperspirant.
Eoux
FDA Label NDC 66854-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Spai Sons Pharmaceutical International Cosmetics for the product Eoux (NDC 66854-009). 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, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Eoux is an anti-bacterial and antiperspirant high protection modern biotechnical design deodorant.
Otc - Keep Out Of Reach Of Children
This product must be keep out reach of the children.
Indications & Usage
This product is designed for use in armpit areas as may cause irritation in the area of application by the sensitivity of the user.
Warnings
Hypersensivity may result in the area of application, not consume this product, if swallowed consult your doctor.
Dosage & Administration
This product is topical application apply the amount necessary in desirable area and rub gently.
Inactive Ingredient
The design of this product does humectant agents to give best feeling in the skin effect in addition to produce antiperspirant and deodorant.
Package Label.Principal Display Panel
IMAGE OF THE LABEL
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