Freshscent Anti-perspirant Deodorant Solution
FDA Label NDC 51824-021

11 label sections · Submitted to the FDA by New World Imports, Inc. · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by New World Imports, Inc. for the product Freshscent Anti-perspirant Deodorant (NDC 51824-021). 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 other, active ingredient, purpose, use, warnings, otc - keep out of reach of children, otc - do not use, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

Drug Facts

Active Ingredient

Aluminum Chlorohydrate 10% –
Anhydrous Basis

Purpose

Antiperspirant

Use

Reduces underarm wetness.

Warnings

For external use only.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.  If accidentally swallowed get medical help or contact a Poison Control Center right away.

Otc - Do Not Use

Do not use on broken skin.

Otc - Stop Use

Stop use if rash or irritation occurs.

Otc - Ask Doctor

Ask a doctor before use if you havekidney disease.

Directions

Apply to underarms only.

Inactive Ingredients

Purified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Fragrance, Tetrasodium EDTA

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