Snp My First Hand Sanitizer
FDA Label NDC 70142-112

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sd Biotechnologies Co., Ltd for the product Snp My First Hand Sanitizer (NDC 70142-112). 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, warnings, keep out of reach of children, uses, directions, inactive ingredient, package label - snp my first hand sanitizer 500ml, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Active ingredients: Ethanol 70%

Purpose

Purpose: Hand Sanitizer

Warnings

Warnings:

• Flammable. Keep away from fire or flame.
• For external use only.
• When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
• Stop use and ask a doctor if irritation or rash appears
and lasts.
• Keep out of reach of children and pets.
• Do not eat.
• If swallowed, get medical help or contact a Poison Control Center right away.

Keep Out Of Reach Of Children

Keep out of reach of children.

Uses

Uses:
Hand sanitizer to help reduce germs on the skin

Directions

Directions:
• Apply a dime sized amount of hand sanitizer to the palm of one hand. Rub hands together covering all surfaces of hands and fingers until dry.
• Children under 6 years of age should be supervised when using. Not recommended for infants.

Inactive Ingredient

Inactive ingredients:

Glycyrrhiza Extract, Green Tea Extract, Rosemary Extract, Butylene Glycol, Aloe Extract(09), Water, Carbomer, Triethanolamine

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