Alcohol
FDA Label NDC 67151-404

12 label sections · Submitted to the FDA by Progressive Products, Llc · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Progressive Products, Llc for the product Alcohol (NDC 67151-404). 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 ingredients, purpose, uses, warnings, otc - do not use section, otc - stop use section, otc - keep out of reach of children section, other warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Alcohol 65.9% by volume

Purpose

Antiseptic

Uses

  • For hand sanitizing to decrease the bacteria on the skin.
  • Apply topically to the skin to help prevent cross contamination
  • Recommended for repeated use.
  • Dries in seconds.

Warnings

  • Flammable, keep away from fire or flame.
  • For external use only.

Directions

  • Remove lid.
  • Pull wipe from center of the roll and thread through opening in lid. Do not push finger through the opening.
  • Replace lid, pull wipe up, and than out at a 45 th angle. The next wipe dispenses automatically.
  • Close lid to retain moisture.

Other Information

Lot No. and Expiration Date can be found on the canister.

Inactive Ingredients

Water, Propylene Glycol, Glycerin, Carbomer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate.

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