NEW EGOROUND HAND SANITIZER- alcohol gel

NEW EGOROUND HAND SANITIZER by

Drug Labeling and Warnings

NEW EGOROUND HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by KMPHARMACEUTICAL Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: ALCOHOL 70.0%

INACTIVE INGREDIENT

Inactive Ingredients:

Water, Glycerin, Butylene Glycol, Aloe Barbadensis Leaf Extract, Carbomer, Triethanolamine, Flavor

PURPOSE

Purpose: SANITIZER

WARNINGS

Warnings:

Flammable. Keep away from fire or flame.
For external use only.

When using this product
do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.

Discontinue use if
irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

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.

Uses

Uses:
Hand sanitizer to help reduce bacteria on the skin.

Directions

Directions:
Put enough product in your palm to cover hands and rub hands together briskly until dry.
Children under 6 years of age should be supervised when using this product.

Other Information

Other Information:
Store below 90°F(32°C)
May discolor certain fabrics or surfaces

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEW EGOROUND HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50555-070
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	350 mL  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Butylene Glycol (UNII: 3XUS85K0RA)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50555-070-01	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2020

Labeler - KMPHARMACEUTICAL Co.,Ltd. (688679158)

Registrant - KMPHARMACEUTICAL Co.,Ltd. (688679158)

Establishment
Name	Address	ID/FEI	Business Operations
KMPHARMACEUTICAL Co.,Ltd.		688679158	manufacture(50555-070)