Hand Sanitizer
FDA Label NDC 78126-008

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Rainhome Pharm&tech Co., Ltd for the product Hand Sanitizer (NDC 78126-008). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredient(s)

→ Purpose

→ Use

→ Warnings

→ Do Not Use

→ Otc - When Using

→ Otc - Stop Use

→ Otc - Keep Out Of Reach Of Children

→ Directions

→ Other Information

→ Inactive Ingredients

→ Package Label - Principal Display Panel

Active Ingredient(S)

Ethyl Alcohol 75% v/v.

Purpose

Antimicrobial.

Use

For handwashing to decrease bacteria on the skin.
recommended for repeated use.

Warnings

For external use only.
FLAMMABLE. KEEP AWAY FROM FLAME.
Do not use in the eyes. In case of contact, rinse eyes thoroughly with wafer.
Stop use, and ask a doctor_ if irritation and redness developand persist for more than 72 hours.
Keep out of reach of children. If swallowed, get medical helpor contact a Poison Control Center right away.

Do Not Use

Do not use in the eyes.

Otc - When Using

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.