PHARMACY PRESCRIPTION 1.8OZ HAND SANITIZER - SWEET PEACH- alcohol gel

PHARMACY PRESCRIPTION 1.8OZ HAND SANITIZER - SWEET PEACH by

Drug Labeling and Warnings

PHARMACY PRESCRIPTION 1.8OZ HAND SANITIZER - SWEET PEACH by is a Otc medication manufactured, distributed, or labeled by Ningbo Liyuan Daily Chemical Products Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62.0%

Purpose

Antimicrobial

Uses

- Helps reduce bacteria on the skin that could cause disease.

Recommended for repeated use.

Warnings

For external use only.

Flammable. Keep away from fire or flame.

When using this product

do not use in or near the eyes. In case of eye contact, flush eyes thoroughly with water.

Stop use and ask a doctor if:

irritation and redness develops and lasts more than 72 hours.

Keep out of reach of children.

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

Directions-

Place enough product in palm to thoroughly cover your hands. Rub hands together briskly until dry.

Children under 6 years of age should be supervised when using this product.

OTHER SAFETY INFORMATION

Other information: Store below 110 Fahrenheit degree (43 degrees Celsius)

May discolor certain fabrics or surfaces.

Inactive Ingredients:

Water, Aloe Barbadensis Gel, Carbomer, Fragrance, Glycerin, Triethanolamine, Tocopheryl Acetate, (Sweet Peach FD&C Red No. 40, FD&C Yellow No. 5)

Drug Facts

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PHARMACY PRESCRIPTION 1.8OZ HAND SANITIZER - SWEET PEACH 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76176-072
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 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: 76176-072-01	53 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/01/2018

Labeler - Ningbo Liyuan Daily Chemical Products Co.,Ltd. (530766098)

Registrant - Ningbo Liyuan Daily Chemical Products Co.,Ltd. (530766098)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Liyuan Daily Chemical Products Co.,Ltd.		530766098	manufacture(76176-072)