FDA.reportPublic FDA data

SaliSkin Wash

Manufacturer
Scientific Solutions Global LLC
Effective date
2019-10-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:00:44

Label at a glance#

ProductSaliSkin Wash
Active ingredientSALICYLIC ACID
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SaliwashSaliwash

OTC - ACTIVE INGREDIENT SECTION

SALICYLIC ACID, TEA TREE OIL

INACTIVE INGREDIENT SECTION

CARBOMER, XANTHAM GUM, TRIETHANOLAMINE, ALOE VERA, MINERAL OIL, PROPYLENE GLYCOL, POLYSORBATE 80, PRESERVED WATER, METHYLPARABEN, PROPYLPARABEN, POLYETHYLENE GLYCOL 400

DOSAGE & ADMINISTRATION SECTION

USE 5-6 PRIOR TO CHEMICAL PEEL.

DISPENSE A DIME-SIZED AMOUNT AND APPLY TO SKIN.

SPEND EXTRA TIME ON PROBLEM AREAS

RINSE USING WARM WATER.

USE AT LEAST 2-3 TIMES A WEEK FOR 12 WEEKS FOR OPTIMAL RESULTS

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

AVOID CONTACT TO EYES.

KEEP OUT OF REACH OF CHILDREN.

STOP USE AND CONSULT DOCTOR IF CONDITION WORSENS OR CLEARS UP AND REOCCURS

OTC - PURPOSE SECTION

REDUCES PORES

BLACKHEADS

REMOVE CYSTIC ACNE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE SECTION

REDUCES PORES

BLACKHEADS

REMOVE CYSTIC ACNE

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71718-501-012021-01-29C16284748780-1ba0f9c33-3da4-a910-e053-dadaa90a0b85941ba3e4-f5b3-1961-e053-2995a90af12b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71718-501-01SaliSkin Wash113 g in 1 BOTTLE, DISPENSINGGEL1131

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71718-501SALISKIN WASH (SALICYLIC ACID) GEL [SCIENTIFIC SOLUTIONS GLOBAL LLC]1Legacy NDC, 1 package rows20191008_941ba3e4-f5b3-1961-e053-2995a90af12b.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71718-50171718-501-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9804Q93RCW27EIACT
XANTHAN GUMTTV12P4NEEIACT
ALOE VERA LEAF POLYSACCHARIDESW21O437517IACT
MINERAL OILT5L8T28FGPIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
POLYSORBATE 806OZP39ZG8HIACT
WATER059QF0KO0RIACT
METHYLPARABENA2I8C7HI9TIACT
PROPYLPARABENZ8IX2SC1OHIACT
TEA TREE OILVIF565UC2GIACT
SALICYLIC ACIDO414PZ4LPZACTIB
TROLAMINE9O3K93S3TKIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT

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
941ba3e4-f5b4-1961-e053-2995a90af12b941ba3e4-f5b3-1961-e053-2995a90af12b2019-10-04WarningsExact identifier
spl id: 941ba3e4-f5b4-1961-e053-2995a90af12b
spl set id: 941ba3e4-f5b3-1961-e053-2995a90af12b

Reported adverse events (FAERS/openFDA)#

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