ANTI BACTERIAL MOISTURIZING HAND SANITIZER CHAMPAGNE TOAST- alcohol gel

Anti Bacterial Moisturizing Hand Sanitizer by

Drug Labeling and Warnings

Anti Bacterial Moisturizing Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Bath & Body Works, Inc., KDC US Holdings, Inc, Memphis Contract Packaging. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 70%

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), Dimethicone, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Isopropyl Myristate, Hydroxypropylcellulose, Aminomethyl Propanol, Mannitol, Cellulose, Dimethiconol, Laureth-4, Laureth-23, Tocopheryl Acetate, Butyrospermum Parkii (Shea) Butter Extract, Aloe Barbadensis Leaf Juice, Silica, Kaolin, Retinyl Palmitate, Caprylic/Capric Triglyceride, Hydroxypropyl Methylcellulose, Titanium Dioxide (CI 77891), Ultramarines (CI 77007).

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 MOISTURIZING HAND SANITIZER  CHAMPAGNE TOAST
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62670-6677
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 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: 62670-6677-0	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/06/2024	05/06/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/06/2024	05/06/2026

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

Establishment
Name	Address	ID/FEI	Business Operations
KDC US Holdings, Inc		080783283	manufacture(62670-6677)

Establishment
Name	Address	ID/FEI	Business Operations
Memphis Contract Packaging		117443103	manufacture(62670-6677)