FDA.reportPublic FDA data

Skinprint Blemish Control Toner

Manufacturer
The Skin Atelier, Inc.
Effective date
2017-11-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:09:32

Label at a glance#

ProductSkinprint Blemish Control Toner
Active ingredientSALICYLIC ACID
Label structure9 sections

Label contents#

Full prescribing information#

INSTRUCTIONS FOR USE SECTION

Use twice daily. Apply after washing face, avoiding the eyes.

DOSAGE & ADMINISTRATION SECTION

Use twice daily. Apply after washing face, avoiding the eyes.

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

Deep cleans while salicylic acid removes and controls excess oils and gently exfoliates away dead skin cells.

OTC - PURPOSE SECTION

Deep cleans while salicylic acid removes and controls excess oils and gently exfoliates away dead skin cells.

INACTIVE INGREDIENT SECTION

ALCOHOL SD 39C, WATER, GLYCERIN, GLYCOLIC ACID, SODIUM HYALURONATE, SALICYLIC ACID, CAPRYLHYDROXAMIC ACID, CAPRYLYL GLYCOL, FRAGRANCE, BLUE #1

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Salicylic Acid 2%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Blemish_Toner_back_OL copy.jpgBlemish_Toner_back_OL copy.jpgBlemish_Toner_front_OL copy.jpgBlemish_Toner_front_OL copy.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71393-00871393-008-07, 71393-008-16

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCOLIC ACID0WT12SX38SIACT
SALICYLIC ACIDO414PZ4LPZACTIB
HYALURONATE SODIUMYSE9PPT4THIACT
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CAPRYLYL GLYCOL00YIU5438UIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
9c58daad-381a-a602-e053-2a95a90a2f93592b1faa-723c-e1f2-e053-2991aa0a2c652020-01-17WarningsExact identifier
spl set id: 592b1faa-723c-e1f2-e053-2991aa0a2c65

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.