Anti-bacterial Hand Sanitizer
FDA Label NDC 62670-6191

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bath & Body Works, Inc. for the product Anti-bacterial Hand Sanitizer (NDC 62670-6191). 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, warnings, flammable, when using this product, stop use and ask a doctor, 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

→ Purpose

→ Use

→ Warnings

→ Flammable

→ When Using This Product

→ Stop Use And Ask A Doctor

→ Keep Out Of Reach Of Children

→ Directions

→ Inactive Ingredients

→ Company Information

→ Product Packaging

Active Ingredient

Alcohol 71%

Purpose

Antiseptic

Use

Decrease bacteria on hands.

Warnings

For external use only.

Flammable

Keep away from flame or high heat.

When Using This Product

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop Use And Ask A Doctor

if irritation and redness develop or increase.

Keep Out Of Reach Of Children

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

Directions

Rub a dime sized drop into hands.

Inactive Ingredients

Water (Aqua, Eau), Fragrance (Parfum),
Carbomer, Lactose, Aminomethyl Propanol, Isopropyl Myristate, Cellulose,
Hydroxyethyl Urea, Tocopheryl Acetate, Wheat Amino Acids, Aloe Barbadensis
Leaf Juice, Butyrospermum Parkii (Shea) Butter Extract, Retinyl Palmitate,
Hydroxypropyl Methylcellulose, Ultramarines (CI 77007).