Sani-maxx Antibacterial Wipes
FDA Label NDC 78915-852

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Tv Direct Llc for the product Sani-maxx Antibacterial Wipes (NDC 78915-852). 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, active ingredients, purpose, warnings:, directions for use:, inactive ingredients:, questions?, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%

Purpose

Antiseptic/Hand & Skin Sanitizer

Warnings:

Do not freeze. For external use only. Store at room temperature.

Do not use ears, eyes or mouth.

  • Avoid contact with eyes. In case of contact, flush eyes with water.
  • Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Directions For Use:

Wipe liberally over the hands & body, rub into skin until dry. Recommended for single use.

Inactive Ingredients:

Water (Aqua), Glycerol, Propanediol, Aloe Vera Extract, Amino acid moisturizer, Hexadecylpyridinium Chloride, Chlorphenesin, Vitamin E, Dodecyl polyglucoside, Citric acid, Sodium citrate.

Questions?

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