Instant Hand Sanitizer
FDA Label NDC 74274-005

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 Instant Hand Sanitizer (NDC 74274-005). 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, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol   65%

Purpose

 Antiseptic

Use

For hand Sanitizing

Otc - Keep Out Of Reach Of Children

if swallowed, get medical help or contact a Poison Control Center right away.

Warnings:

Flamable, keep away from heat and flames

For external use only

When using this product

Keep out of eye, In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

Stop and ask a doctor

if skin irritation develops.

Directions

  • Wet hands thoroughly with product and allow to dry without wiping.
  • For children under 6 age use only under adult supervision.
  • Not recommended for infants.

    • Other information

    • Do not store above 105℉。
    • May discolor some fabrics.

Inactive Ingredients

Aqua, glycerin, carbomer, propyene glycol, sodium hydroxide.

* Please review the disclaimer below.