all clear exfoliating face wash

Manufacturer
Virgin Scent Inc.
Effective date
2021-12-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:46:12

Label at a glance#

Productall clear exfoliating face wash
Active ingredientSALICYLIC ACID
Label structure7 sections

Dosage and administration

• Clean the skin thoroughly before applying this product • Cover the entire affected area with a thin layer and rinse thoroughly one to three times daily • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor • If bothersome dryness or peeling occurs, reduce application to once a day or every

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

Acne medication

Use

INDICATIONS & USAGE SECTION

For the treatment of acne

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

• skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

Keep out if reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Clean the skin thoroughly before applying this product
• Cover the entire affected area with a thin layer and rinse thoroughly one to three times daily
• Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
• If bothersome dryness or peeling occurs, reduce application to once a day or every

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), sodium hydroxide, pentylene glycol, propanediol, glycolic acid, dimethylisosorbide, gluconolactone, xanthan gum, sodium benzoate

Questions?

OTC - QUESTIONS SECTION

info@artnaturals.com
Customer service: 855-art-4488

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
562600salicylic acid 2 % Medicated Liquid SoapPSN1
562600salicylic acid 20 MG/ML Medicated Liquid SoapSCD1
562600salicylic acid 2 % Facial Cleanser TonerSY1
562600salicylic acid 2 % Facial ScrubSY1
562600salicylic acid 2 % Medicated Liquid SoapSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78706-006-002023-01-30C16284748780-1f386c64a-180d-0266-e053-dadaa90a7c1aall clear exfoliating face wash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78706-006-00all clear exfoliating face wash113 g in 1 BOTTLE, PLASTICPASTE1131

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78706-006ALL CLEAR EXFOLIATING FACE WASH (SALICYLIC ACID) PASTE [VIRGIN SCENT INC.]1Legacy NDC, 1 package rows20220101_c3845fec-5f4f-4bce-8953-254931035e64.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78706-00678706-006-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
d3a688af-22a0-9ff5-e053-2a95a90afafec3845fec-5f4f-4bce-8953-254931035e642021-12-21WarningsExact identifier
spl id: d3a688af-22a0-9ff5-e053-2a95a90afafe
spl set id: c3845fec-5f4f-4bce-8953-254931035e64

Reported adverse events (FAERS/openFDA)#

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