QYO QYO Tangerine Bright Moist Peeling Pack: Package Insert and Label Information

QYO QYO TANGERINE BRIGHT MOIST PEELING PACK- kaolin paste
LaLa Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

ACTIVE INGREDIENTS

KAOLIN 5%

PURPOSE

SKIN PROTECTANT

USES

• Helps prevent and temporarily protects chapped or cracked skin.

WARNINGS

For external use only.

When using this product • do not get into eyes.

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. 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

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 DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KAOLIN (KAOLIN) KAOLIN 5 g in 100 mL

Inactive Ingredients Ingredient Name Strength STEARIC ACID BUTYLENE GLYCOL TANGERINE PEEL WATER GLYCERIN BENTONITE POTASSIUM HYDROXIDE SODIUM LAURYL SULFATE

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:71733-108-01 1 JAR in 1 BOX contains a JAR 1 100 mL in 1 JAR This package is contained within the BOX (71733-108-01)

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	Operations
LaLa Co., Ltd.		694617781	manufacture (71733-108)

Revised: 01/2019 LaLa Co., Ltd.