Hand Sanitizer
FDA Label NDC 70675-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Deqing Jiarou Daily Chemical Co., Ltd for the product Hand Sanitizer (NDC 70675-001). 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 other, active ingredient, purpose, otc - keep out of reach of children, uses, warning, directions, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Other

→ Active Ingredient

→ Purpose

→ Otc - Keep Out Of Reach Of Children

→ Uses

→ Warning

→ Directions

→ Other Safety Information

→ Inactive Ingredients

→ Packaging

Other

Drug Facts

Active Ingredient

Ethyl Alcohol 62.0%

Purpose

Antimicrobial

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.Children must be supervised in use of this product.

Uses

Hand sanitizer to help decrease bacteria on the skin.
When water, soap & towel are not available.
Recommended for repeated use.

Warning

For external use only.
Flammable.Keep away from fire or flame.
Do not apply around eyes.Do not use in ears & mouth.
When using this product, avoid contact with eyes. In case of contact flush eyes with water.
Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.