Maximum Strength Acne Spot Treatment

Manufacturer
CVS | Product Quest Mfg
Effective date
2018-06-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:36

Label at a glance#

ProductMaximum Strength Acne Spot Treatment CVS Health
Active ingredientBenzoyl Peroxide
Label structure7 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 are sensitive to benzoyl peroxide
When using this product • 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.
• 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 skin
irritation becomes severe

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions • cleanse the skin
thoroughly before applying medication
• cover the entire affected area with a thin
layer one to three times a day • 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 other day. • if going
outside, use a sunscreen. Allow product to
dry, then follow direction in the sunscreen
labeling. If sensitivity develops, discontinue
use of both products and consult a doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients
Aluminum Hydroxide,
Bentonite, Carbomer, Glyceral
Stearate, Isopropyl Myristate,
PEG-12, Potassium Hydroxide,
Potassium Sorbate, Propylene
Glycol, Water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
106315benzoyl peroxide 10 % Topical CreamPSN1
106315benzoyl peroxide 100 MG/ML Topical CreamSCD1
106315benzoyl peroxide 10 % Topical CreamSY1

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
69842-674-012020-01-31C16284748780-19d75b9cf-fa13-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-674-01Maximum Strength Acne Spot TreatmentCVS Health28 g in 1 TUBECREAM281

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-674MAXIMUM STRENGTH ACNE SPOT TREATMENT CVS HEALTH (BENZOYL PEROXIDE 10%) CREAM [CVS]1Legacy NDC, 1 package rows20180815_e617eca2-8aa7-41bb-9391-b309aa4a6aab.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-67469842-674-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
89e25222-8fcb-4a04-a31c-672a1610ffade617eca2-8aa7-41bb-9391-b309aa4a6aab2018-06-05WarningsExact identifier
spl id: 89e25222-8fcb-4a04-a31c-672a1610ffad
spl set id: e617eca2-8aa7-41bb-9391-b309aa4a6aab

Reported adverse events (FAERS/openFDA)#

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