Anti-bacterial Hand
FDA Label NDC 62670-5921

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 (NDC 62670-5921). 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 the 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 The Reach Of Children

→ Directions

→ Inactive Ingredients

→ Company Information

→ Product Packaging

Active Ingredient

Alcohol (72%)

Purpose

Antiseptic

Use

To decrease bacteria on skin.

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.

Keep Out Of The Reach Of Children

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

Directions

Spray hands thoroughly.
Rub until dry.

Inactive Ingredients

INACTIVE INGREDIENTS: Water (Aqua, Eau), PEG-12 Dimethicone, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane, Butylene Glycol, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Cocos Nucifera (Coconut) Fruit Extract, Honey Extract (Mel, Extrait de miel), Olea Europaea (Olive) Fruit Extract.