Antiperspirant Wipe For Women Swab
FDA Label NDC 71592-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Flawlesswipes, Llc for the product Antiperspirant Wipe For Women (NDC 71592-001). 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, pakaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Aluminum Chlorohydrate 15%

Purpose

Antiperspirant

Uses

Underarm antiperspirant to reduce perspiration and odor

Warnings

  • For external use only
  • When using this product avoid contact with eyes. in case of eye contact, flush thoroughly with water.
  • Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a poison control center right away

Directions

Open packet, remove and unfold wipe, apply to underarm only, dispose of used wipe in the trash, do not flush.

Inactive Ingredients

Water, polysorbate 20, Salvia Officinalis (Sage) Leaf Extract, Usnea Barbata (Lichen) extract, Tocopherol, Tocopheryl Acetate, PEG-180, Phenoxyethanol, Benzyl Alcohol, Potassium Sorbate, Fragrance

* Please review the disclaimer below.