ANTI-BACTERIALHANDSPRAY WINTER CANDY APPLE- alcohol spray

Anti-BacterialHandSpray by

Drug Labeling and Warnings

Anti-BacterialHandSpray by is a Otc medication manufactured, distributed, or labeled by Bath & Body Works, Inc., KDC US Holdings, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 72%

Purpose

Antiseptic

Use

Decreases bacteria on hands.

Warnings

Flammable. Keep away from flame or high heat.

WARNINGS

For external use only.

WHEN USING

When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation and redness develop.

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, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Hexamethylindanopyran, Citrus Aurantium Peel Oil, Limonene, Hexyl Cinnamal, Vanillin, Citronellol, Linalool, Acetyl Cedrene, Tetramethyl Acetyloctahydronaphthalenes, Geranyl Acetate, Amyl Cinnamal, Geraniol, Terpineol, Benzyl Salicylate, Eugen, Red 40 (CI 16035), Red 33 (CI 17200), Yellow 5 (CI 19140), Ext. Violet 2 (CI 60730).

SPL UNCLASSIFIED SECTION

Bath & Body Works Distr., 95 West Main Street

New Albany, OH 43054, 1-800-395-1001

pat. www.bbwinc.com/patents

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTI-BACTERIALHANDSPRAY  WINTER CANDY APPLE
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62670-6986
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62670-6986-2	29 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/20/2025	10/20/2027

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/20/2025	10/20/2027

Labeler - Bath & Body Works, Inc. (878952845)

Establishment
Name	Address	ID/FEI	Business Operations
KDC US Holdings, Inc.		080783283	manufacture(62670-6986)