Advanced 3 in 1 Exfoliating Cleanser

Manufacturer
CVS | Product Quest Mfg.
Effective date
2017-12-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:53:19

Label at a glance#

ProductAdvanced 3 in 1 Exfoliating Cleanser
Active ingredientBENZOYL PEROXIDE
Label structure6 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                                  Purpose
Benzoyl Peroxide 5%.............................................Acne Treatment

INDICATIONS & USAGE SECTION

Use For the treatment of acne.

WarningsFor external use only

WARNINGS SECTION

Do not use if you have very sensitive skin or if you are sensitive to benzoyl peroxide.
When using this product • skin irritation and dryness are 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. • rinse right away with water if it gets in
eyes • avoid unnecessary sun exposure and use a sunscreen • avoid contact with the eyes, lips, and mouth • avoid contact with
hair and dyed fabrics, which may be bleached by this product • skin irritation may occur, characterized by redness, burning,
itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.
Stop use and ask a doctor if irritation becomes severe.

DOSAGE & ADMINISTRATION SECTION

Directions • Wet face • Apply to hands and work into a lather • Massage face gently • Rinse thoroughly and pat dry • Cleanse
twice a day • If going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and consult a doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water,
Polyacrylamide, C13-14 Isoparaffin,
Cocamidopropyl Betaine, Jojoba Esters,
Laureth-7, Phenoxyethanol,
Ethylhexylglycerin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308696benzoyl peroxide 5 % Medicated Liquid SoapPSN2
308696benzoyl peroxide 50 MG/ML Medicated Liquid SoapSCD2
308696benzoyl peroxide 5 % Medicated Liquid SoapSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130050428435663GTIN-13: 0050428435663
EAN-13: 0050428435663
GTIN-12: 050428435663
UPC-A: 050428435663
GTIN storage (14 digits): 00050428435663
label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a46239a7-5963-4008-8cbb-6b9000f497ebProduct name120250721
b382b4e1-6b48-45f6-bffc-e61b00b0ce19Product name320250317
d9d61457-6a5a-41fc-b418-e5479a2904b7Product name220230303
32012d5c-25ac-49c7-9d4c-1313177fff7cProduct name120230112
13e7e7e3-e885-4c79-af6d-dad1aedbb06eProduct name120220128
4a7d44fe-774d-404b-aad0-8a90fe78375aProduct name420211025
3f45980c-c196-47e5-0e5e-48b7c57327c5Product name520200428
d12e2d7c-bd6b-45d4-94f9-6df8e1b8b27bProduct name320200203
ee5c6de5-d9cd-454f-b250-7b19e5cf2992Product name420190619
ad75fcfd-a339-42a1-9c60-43ba2c654cfaProduct name120170810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69842-839-042020-01-31C16284748780-19d75b9d0-f286-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-839-04Advanced 3 in 1 Exfoliating Cleanser148 mL in 1 TUBECREAM1482

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-839ADVANCED 3 IN 1 EXFOLIATING CLEANSER (BENZOYL PEROXIDE 5.0%) CREAM [CVS]2Legacy NDC, 1 package rows20171208_50d0909f-4ebe-47cc-8005-996695d0ff08.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-83969842-839-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML · Source PDF

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
63789548-fe35-435f-82a9-1b4aa2ecc97450d0909f-4ebe-47cc-8005-996695d0ff082017-12-08WarningsExact identifier
spl id: 63789548-fe35-435f-82a9-1b4aa2ecc974
spl set id: 50d0909f-4ebe-47cc-8005-996695d0ff08

Reported adverse events (FAERS/openFDA)#

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