M Marvel Sani Care Instant Hand Sanitizer
FDA Label NDC 80107-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Techin Development Co., Ltd for the product M Marvel Sani Care Instant Hand Sanitizer (NDC 80107-001). 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 active ingredient, purpose, use, warnings, otc - when using, otc - stop use, otc - keep 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

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use

For daily hand sanitizing, to reduce bateria on hands

Warnings

For external use only

Flammable. Keep away from fires and high temperature

Otc - When Using

Do not use on open skin wounds

Avoid eyes. In case of contact with eyes, rinse eyes thoroughly with water.

Otc - Stop Use

Stop use if irritation or rash occurs, if condition persists, contact a healthcare proactitioner

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.

Directions

  • Put proper amount onto palms and rub hands briskly until dry.
  • No washing or rinsing required. Air dries quickly

Other Information

Keep in closed container in a cool dry place of ambient temperature between 5-30C (59-86F)

Batch and MFG date printed on bottle

Validity: 24 mounths from MFG date

Made in China

Inactive Ingredients

Water, Aminomethyl propanol, aloe vera extract, glycerin, carbomer, D-Panthenol, vitamin E

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