Magicare Premium Hand Sanitizing Wipes Cloth
FDA Label NDC 85276-104

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Magicare Tech Corp for the product Magicare Premium Hand Sanitizing Wipes (NDC 85276-104). 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 drug facts, active ingredient, purpose, uses, warnings:, do not use, stop use and consult with a physician, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

ETHYL ALCOHOL 75%

Purpose

ANTIMICROBIAL

Uses

HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN.

Warnings:

FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME. • FOR EXTERNAL USE ONLY.

Do Not Use

  • IN OR NEAR THE EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.

Stop Use And Consult With A Physician

IF IRRITATION DEVELOPS AND LASTS FOR MORE THAN 72 HOURS.

Keep Out Of Reach Of Children.

  • IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

Directions:

STORAGE: STORE AT ROOM TEMPERATURE.

  • DISPENSING: LIFT THE FRONT LID. OPEN PROTECTIVE SEAL. PULL OUT WIPE, RESEAL, AND CLOSETHE LID. 
  • USE: WIPE HANDS THOROUGHLY.
  • DISPOSAL: DO NOT FLUSH.

Inactive Ingredients:

PURIFIED WATER

Package Labeling: 20 Count

Label (Label)

Label (Label)

Package Labeling: 80 Count

Label2 (Label2)

Label2 (Label2)

Package Labeling: 100 Count

Label3 (Label3)

Label3 (Label3)

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