SKINPRINT CLEARTONE WITH 2% HYDROQUINONE- skinprint cleartone with 2% hydroquinone liquid
The Skin Atelier, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Directions

Directions: Apply a small amount to a cotton pad and apply to a pigmented area after cleansing. Then apply Skinprint Illuminate or Recover Lighteners for optimal results.

Directions

Directions: Apply a small amount to a cotton pad and apply to a pigmented area cleansing. Then apply Skinprint Illuminate or Recover lighteners for optimal results.

Warning

For external use only. When using this product avoid contact with eyes. If contact occurs flush thoroughly with water. Keep out of reach of children. If swallowed get medical help or contact Poison Control right away.

Inactive Ingredients:

ALCOHOL SD 40B, WATER, GLYCERIN, CAMELLIA SINENSIS (TEA) EXTRACT (AND) ASPALATHUS LINEARIS (ROOIBOS) EXTRACT (AND) BOSWELLIA SERRATA EXTRACT (AND) HONEY EXTRACT (AND) TETRAPEPTIDE-14 (AND) PHENOXYETHANOL (AND) SODIUM BENZOATE, DISODIUM EDTA, SODIUM METABISULFITE, BLUE #1

Indications & Usage Section

This pigment clearing booster helps to clear all types of dark spots from skin. It should be used as a spot treatment with Skinprint Illuminate or Recover skin lighteners.

OTC- PURPOSE SECTION

This pigment clearing booster helps clear all types of dark spots from skin. It should be used as a spot treatment with Skinprint Illuminate or Recover skin lighteners.

OTC- KEEP OUT OF REACH OF CHILDREN SECTION

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

Active Ingredient

Active Ingredient: 2% HYDROQUINONE

Product Name

Product Label

SKINPRINT CLEARTONE WITH 2% HYDROQUINONE
skinprint cleartone with 2% hydroquinone liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71393-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	0.02 g in 1 g

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
HONEY (UNII: Y9H1V576FH)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
ACETYL TETRAPEPTIDE-15 (UNII: 6K389LE0MV)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM BENZOATE (UNII: OJ245FE5EU)
BOSWELLIA SERRATA WHOLE (UNII: X7B7P649WQ)
DISODIUM HEDTA (UNII: KME849MC7A)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71393-001-02	60 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/02/2013

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		12/02/2013	10/11/2019

Labeler - The Skin Atelier, Inc. (135049810)

Name	Address	ID/FEI	Business Operations
Establishment
The Skin Atelier, Inc.		135049810	manufacture(71393-001)

Revised: 1/2020

Document Id: 9c58e93d-c518-578b-e053-2995a90ab4f6

Set id: 4ce57287-184a-4b5b-e054-00144ff8d46c

Version: 2

Effective Time: 20200117

The Skin Atelier, Inc.