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.

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Qyo Qyo Tangerine Bright + Moist
Peeling Pack

ACTIVE INGREDIENTS

KAOLIN 5%

PURPOSE

SKIN PROTECTANT

USES

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

peelingpack

QYO QYO TANGERINE BRIGHT MOIST PEELING PACK 
kaolin paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71733-108
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
KAOLIN (UNII: 24H4NWX5CO) (KAOLIN - UNII:24H4NWX5CO) KAOLIN5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71733-108-011 in 1 BOX01/01/2018
1100 mL in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34701/01/2018
Labeler - LaLa Co., Ltd. (694617781)
Establishment
NameAddressID/FEIBusiness Operations
LaLa Co., Ltd.694617781manufacture(71733-108)

Revised: 1/2019
Document Id: 94ede99d-bedb-1b3c-e053-2a95a90a0fa4
Set id: 94edf1d0-cdc0-3b52-e053-2a95a90ac86f
Version: 1
Effective Time: 20190101
 
LaLa Co., Ltd.