SaliSkin

Manufacturer
SSG Ventures Inc
Effective date
2021-04-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:40:51

Label at a glance#

ProductSaliSkin
Active ingredientSALICYLIC ACID
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

OTC - ACTIVE INGREDIENT SECTION

SALICYLIC ACID, TEA TREE OIL

INACTIVE INGREDIENT SECTION

MEDIDERM CREAM, GREEN TEA EXTRACT, ALOE VERA, EMULTHIX

DOSAGE & ADMINISTRATION SECTION

WASH FACE THOROUGHLY AND APPLY TO AFFECTED AREAS. USE CONTINUOUSLY FOR AT LEAST 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 REOOCCURS.

OTC - PURPOSE SECTION

REMOVES PIMPLES

MINIMIZES PORES

ENHANCED WITH TEA TREE OIL AND ALOE VERA

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH FO CHILDREN

INDICATIONS & USAGE SECTION

USE CONTINUOUSLY FOR AT LEAST 12 WEEKS FOR OPTIMAL RESULTS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
317152salicylic acid 2 % Topical CreamPSN2
317152salicylic acid 20 MG/ML Topical CreamSCD2
317152salicylic acid 2 % Topical CreamSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81376-500-012023-01-30C16284748780-1f386c649-e5db-0266-e053-dadaa90a7c1aSaliskin

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81376-500-01SaliSkin56 g in 1 JARCREAM562

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81376-500SALISKIN (SALICYLIC ACID) CREAM [SSG VENTURES INC]2Legacy NDC, 1 package rows20210617_b711935a-4167-cefb-e053-2995a90a03db.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81376-50081376-500-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
bf66d0de-71d9-1817-e053-2a95a90a08d9b711935a-4167-cefb-e053-2995a90a03db2021-04-07WarningsExact identifier
spl id: bf66d0de-71d9-1817-e053-2a95a90a08d9
spl set id: b711935a-4167-cefb-e053-2995a90a03db

Reported adverse events (FAERS/openFDA)#

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