Active Ingredient
Alcohol 72%
Anti-bacterialhandspray
FDA Label NDC 62670-6797
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-bacterialhandspray (NDC 62670-6797). 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, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Decreases bacteria on hands.
Warnings
Flammable. Keep away from flame or high heat.
For external use only.
Otc - When Using
When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor is irritation and redness develop.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Spray hands thoroughly.
- Rub until dry.
Inactive Ingredient
Water (Aqua, Eau), Fragrance (Parfum), PEG-12 Dimethicone, Butyrospermum Parkii (Shea) Butter Extract, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Red 33 (CI 17200), Ext. Violet 2 (CI 60730), Yellow 5 (CI 19140).
Other
Bath & Body Works Distr., 95 West Main Street
New Albany, OH 43054, 1-800-395-1001
pat. www.bbwinc.com/patents
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