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

peelingpack

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.

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