Caseys Solution
FDA Label NDC 85844-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Bright Care Co., Ltd. for the product Caseys (NDC 85844-001). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - ask doctor, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredient

BENZALKONIUM CHLORIDE 0.13%

Otc - Purpose

Purpose

Antibacterial

Indications & Usage

Uses

  • To decrease bacteria on the skin
  • Recommended for repeated use

Warnings

Warnings

For external use only.

Otc - When Using

When using this product, keep away from eyes.  In case of eye contact, rinse eyes with water

Otc - Ask Doctor

Stop use and ask a doctor if irritation or redness develops or lasts for more than 72 hours

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions:

  • rub wipe thoroughly over all surfaces of both hands
  • allow to dry without wiping
  • superwise children under 6 years old
  • not recommended for infants
  • dispose of wipe in trash, do not flush

Inactive Ingredient

Inactive ingredients

Water, Fragrance, C12-15 Alcohols, Chloroxylenol, Aloe Barbadensis Leaf Juice

* Please review the disclaimer below.