Hand Sanitizer
FDA Label NDC 74274-008

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Huizhou Bliss Commodity Co., Ltd for the product Hand Sanitizer (NDC 74274-008). 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 active ingredient, purpose, use, otc - keep out of reach of children, warnings:, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 75%

Purpose

Sanitizer

Use

  • to decrease bacteria on the skin that could cause disease.
  • recommended for repeated use.

Otc - Keep Out Of Reach Of Children

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Warnings:

Flamable, keep away from heat and flame

For external use onl-hands. Use only as directed. Excessive use or prolonged exposure may cause irritation to skin. Discontinue use if rash, redness or itching occurs.

When using this product

  • keep out of eyes, in case of contact with eyes, immediately flush with water and call a doctor.
  • avoid contact with broken skin

    • Stop use and ask a doctor if Irritation and redness develops

Directions

put a thumb size amount in your palm and rub hands together briskly until dry.

Other Information

  • do not store in temperatures over 118℉
  • children under 6 years of age should be supervised while using this product
  • may discolor certain fabrics

Inactive Ingredients

Water, glycerin, propyene glycol, carbomer, sodium hydroxide

* Please review the disclaimer below.