Germisept Antibacterial Alcohol Wipes
FDA Label NDC 75127-008

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Jurong Dongfa General Merchandise Co., Ltd. for the product Germisept Antibacterial Alcohol Wipes (NDC 75127-008). 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 drugs fact, active ingredient, purpose, uses:, warnings, do not use, keep this 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

Drugs Fact

Active Ingredient

Ethyl Alcohol 75%(v/v)

Purpose

Antiseptic

Uses:

  • For cleansing to decrease bacteria on skin.
  • Recommended for repeated use with a new unused wipe each time.
  • Dries quickly.

Warnings

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

Do Not Use

  • in or contact the eyes.
  • Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a physician.

Keep This Out Of Reach Of Children.

  • unless under adult supervision.
  • If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

  • Open the flip top lid, remove one wipe to use.
  • Wipe hands thoroughly with product and allow to dry without wiping.
  • Close filp top lid label after use to retain moisture.

Other Information

  • Dispose of wipe in the proper container.
  • Do not flush down the toilet.

Inactive Ingredients

Aloe Barbadensis Leaf Extract, Aqua (Purified & De-Ionized Water), Benzalkonium Chloride, Glycerin.

Package Labeling:

1 (008)

1 (008)

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