Freshorize
FDA Label NDC 52305-500

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Freshorize, Ltd. for the product Freshorize (NDC 52305-500). 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 lngredient, purpose, uses, warnings, directions, inactives, keep out of reach of children., other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Lngredient

Ethyl Alcohol 70 %v/v

Purpose

Hand wipes

Uses

For handwashing to decrease bacteria on the skin - recommended for repeated use

Warnings


For external use only.

Flammable. Keep away from fire or flame.

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation and redness develop and 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

Tear open packet, unfold and use wipe on surface or hands.

Allow to air dry without washing

Supervise children under 6 years in the use of this product

Inactives

Water (Aqua)

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Other Information

  • Store at 20°C to 25°C (68° to 77°F)
  • May discolor certain fabrics.

* Please review the disclaimer below.