Antiperspirant Towlette
FDA Label NDC 55726-200

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zero Sweat for the product Antiperspirant Towlette (NDC 55726-200). 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 active ingredient, purpose, uses, warnings, keep out of reach of children, directions, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Aluminum Chloride 14%

Purpose

Antiperspirant

Uses

Reduces underarm perspiration

Warnings

For external use only

Do not use on broken skin

Stop use if rash or irritation occurs

Ask a doctor before use if you have kidney disease

Keep Out Of Reach Of Children

Keep out of reach of children unless under adult supervision. If swallowed get medical help or contact a Poison Control Center right away.

Directions

Apply to underarms only

Inactive Ingredients

Water, Polysorbate 20, PEG-180, Salvia Officionalis (Sage) Leaf Extract, Usnea Barbata (Lichen) Extract, Tocopheryl Acetate, Phenoxyethanol, Ethylhexylglycerin

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