Foamimg Acne Face Wash

Manufacturer
CVS | Product Quest Mfg
Effective date
2018-04-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:16

Label at a glance#

ProductFoamimg Acne Face Wash
Active ingredientBenzoyl Peroxide
Label structure6 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                   Purpose
Benzoyl Peroxide 10%...........................Acne Treatment

INDICATIONS & USAGE SECTION

Use For the treatment of acne

WARNINGS SECTION

Warnings
For external use only.
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 consult 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, Sodium Cocoyl Isethionate, Cetearyl Alcohol, Cocamidopropyl Betaine, Potassium Lauryl Phosphate, Glycerin, Sodium
Hydroxide, Glycolic Acid, Mineral Oil, Lactic Acid, Titanium
Dioxide, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,
Sodium PCA, Sodium Lauryl Sulfoacetate, Disodium Laureth
Sulfosuccinate, Phenoxyethanol, Ethylhexylglycerin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
142034benzoyl peroxide 10 % Medicated Liquid SoapPSN1
142034benzoyl peroxide 100 MG/ML Medicated Liquid SoapSCD1
142034benzoyl peroxide 10 % Medicated Liquid SoapSY1

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
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
3f45980c-c196-47e5-0e5e-48b7c57327c5Product name520200428
d12e2d7c-bd6b-45d4-94f9-6df8e1b8b27bProduct name320200203
ee5c6de5-d9cd-454f-b250-7b19e5cf2992Product name420190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
ad75fcfd-a339-42a1-9c60-43ba2c654cfaProduct name120170810
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69842-666-052020-01-31C16284748780-19d75b9d0-7db0-f424-e053-dadaa90a57ceCVS Health Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-666-05Foamimg Acne Face Wash187 g in 1 TUBECREAM1871

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-666FOAMIMG ACNE FACE WASH (BENZOYL PEROXIDE 10%) CREAM [CVS]1Legacy NDC, 1 package rows20180425_ed4a4a93-f750-4787-9046-55cf37b90eb4.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-66669842-666-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
3efb0c05-2579-4f09-8beb-5916b1d92fcded4a4a93-f750-4787-9046-55cf37b90eb42018-04-24WarningsExact identifier
spl id: 3efb0c05-2579-4f09-8beb-5916b1d92fcd
spl set id: ed4a4a93-f750-4787-9046-55cf37b90eb4

Reported adverse events (FAERS/openFDA)#

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