Sanitizer Wipe In Sachet
FDA Label NDC 69491-035

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Buzz Products Inc for the product Sanitizer Wipe In Sachet (NDC 69491-035). 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, when using this product, stop using and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 75% (v/v)

Purpose

Antiseptic

Uses

  • To help reduce bacteria on the skin.

Warnings

  • For external use only.
  • Do not dispose of wipes in flush toilets.

    • Flammable

    • Keep away from fire or flame.

When Using This Product

  • avoid contact with eyes.
  • If contact occurs, rinse thoroughly with water.

Stop Using And Ask A Doctor If

  • irritation or redness develops and lasts.

Keep Out Of Reach Of Children

  • In case of accidental ingestion, get medical help or contact a poison control center immediately.

Directions

  • Appyl to hands or surface.
  • No rinsing required.
  • Discard after use.

Other Information

  • Store below 110°F (43°C).
  • May discolor certain fabrics or surfaces.

Inactive Ingredients

Aqua (Water), Glycerin, Polyquaternium-37, Melaleuca Alternifolia Leaf Oil.

Package Labeling:

Label (Label)

Label (Label)

* Please review the disclaimer below.