QYO QYO TANGERINE BRIGHT MOIST PEELING PACK- kaolin paste

QYO QYO Tangerine Bright Moist Peeling Pack by

Drug Labeling and Warnings

QYO QYO Tangerine Bright Moist Peeling Pack by is a Otc medication manufactured, distributed, or labeled by LaLa Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

KAOLIN 5%

PURPOSE

SKIN PROTECTANT

USES

• Helps prevent and temporarily protects chapped or cracked skin.

WARNINGS

For external use only.

WHEN USING

When using this product do not get into eyes.

STOP USE

Stop us and ask doctor if condition worsens symptoms last
more than 7 days or clear up and occurs again within a few days.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply as needed. After cleansing your face, apply two spatula of peeling pack and spread evenly on your face. Wait 10 to 15 minutes. Massage and deep cleanse your skin before rinsing with luke warm water.

Inactive Ingredients

Water, Sodium lauryl sulfate, Stearic Acid, Glycerin, Volcanic Ash, Buylene Glycol, Potassium Hydroxide, Bentonite, Betaine

Other Information

Protect this product from excessive heat and direct sun.

Questions or Comments?

Call toll free 1-800-311-6680

PRINCIPAL DISPLAY PANEL Qyo Qyo Tangerine Bright + Moist Peeling Pack 100mL

INGREDIENTS AND APPEARANCE

QYO QYO TANGERINE BRIGHT MOIST PEELING PACK 
kaolin paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71733-108
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KAOLIN (UNII: 24H4NWX5CO) (KAOLIN - UNII:24H4NWX5CO)	KAOLIN	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
STEARIC ACID (UNII: 4ELV7Z65AP)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
TANGERINE PEEL (UNII: JU3D414057)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
BENTONITE (UNII: A3N5ZCN45C)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71733-108-01	1 in 1 BOX	01/01/2018
1		100 mL in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	01/01/2018

Labeler - LaLa Co., Ltd. (694617781)

Establishment
Name	Address	ID/FEI	Business Operations
LaLa Co., Ltd.		694617781	manufacture(71733-108)