Traveltime Instant Hand Sanitizer
FDA Label NDC 74274-007

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 Traveltime Instant Hand Sanitizer (NDC 74274-007). 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

Hand sanitizer to help reduce bacteria on the skin.

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 fire or flame or sparks.

For external use only

When using this product

  • do not use in or near eyes
  • If case of contact, rinse eyes thoroughly with water

    • Stop use and ask a doctor if

    Irritation or rash appears on the skin.

Directions

  • put enough product in palm to cover hands and rub hands together until dry.
  • Children under 6 years of age should be supervised when applying product.

    • Other information:

    • Store below 110° （43℃）
    • May discollor certain fabrics or surfaces.

Inactive Ingredients

Water, glycerin, propyene glycol, carbomer, sodium hydroxide, Aloe Barbadensis Leaf Juice, Fragrance

* Please review the disclaimer below.