Fresh N Up
FDA Label NDC 57624-601

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Rockline Industries, Inc for the product Fresh N Up (NDC 57624-601). 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 use and ask a doctor if, 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 Ingredient

Benzalkonium chloride 0.115%

Purpose

Antibacterial

Uses

For hand washing to decrease bacteria on the skin

Warnings

For external use only

When Using This Product

Avoid the eyes and mucous membranesIf contact occurs, rinse eyes thoroughly with water

Stop Use And Ask A Doctor If

If irritation develops and persists for more than 72 hours.

Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed contact a doctor or Poison Control Center right away.

Other Information

May be used on face, arms and legs.

Directions

  • For use apply thoroughly to hands and face as desired. Allow to dry without wiping. Discard wipe in trash receptacle after use. Do not flush.
  • For dispensing tear open package at notch. Dispose of wrapper in trash. Do  not flush

Inactive Ingredients

Acrylates Copolymer, Benzophenone-4, Citric Acid, Cocamide DEA, Cocamidopropyl Betaine, Disodium EDTA, FDC Yellow 5, FDC Blue 1, Fragrance, Methylchloroisothiazolinone, Methylisothiazolinone, Sodium Chloride, Sodium Laureth Sulfate, Water

Package Label

Package label

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