ANTI BACTERIAL HAND GEL SUNNY COCONUT- alcohol gel

Anti Bacterial Hand Gel by

Drug Labeling and Warnings

Anti Bacterial Hand Gel by is a Otc medication manufactured, distributed, or labeled by Bath & Body Works, Inc., KDC US Holdings, Inc., MCP TN. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 71%

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 keep out of eyes. Stop use and ask a doctor if irritation or redness develops.

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

Rub a dime sized drop into hands.

INACTIVE INGREDIENT

Water (Aqua, Eau), Fragrance (Parfum), Carbomer, Mannitol, Isopropyl Myristate, Cellulose, Hydroxyethyl Urea, Tocopheryl Acetate, Wheat Amino Acids, Aloe Barbadensis Leaf Juice, Butyrospermum Parkii (Shea) Butter Extract, Kaolin, Silica, Hydroxypropyl Methylcellulose, Caprylic/Capric Triglyceride, Retinyl Palmitate, Aminomethyl Propanol, Limonene, Citrus Aurantium Peel Oil, Benzyl Salicylate, Coumarin, Citral, Citrus Limon Peel Oil, Rose Ketones, Cananga Odorata Oil/Extract, Pinene, Ultramarines (CI 77007), Yellow 5 (CI 19140), Red 33 (CI 17200), Red 40 (CI 16035), 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 BACTERIAL HAND GEL  SUNNY COCONUT
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62670-6967
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71 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: 62670-6967-0	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/22/2025	12/22/2028

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/22/2025	12/22/2028

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

Establishment
Name	Address	ID/FEI	Business Operations
KDC US Holdings, Inc.		080783283	manufacture(62670-6967)

Establishment
Name	Address	ID/FEI	Business Operations
MCP TN		117443103	manufacture(62670-6967)