Targeted Acne Spot Treatment

Manufacturer
CVS | Product Quest Mfg, LLC
Effective date
2018-02-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:54:42

Label at a glance#

ProductTargeted Acne Spot Treatment CVS
Active ingredientBENZOYL PEROXIDE
Label structure12 sections

Indications and uses

Treats and helps prevent new acne blemishes.

Dosage and administration

Cleanse skin thoroughly before applying. COver entire affected area with a thin layer 1 to 3 times daily. Start with one application daily, because excessive drying may occur. Then gradually increase to 2 to 3 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 outsie use a sunscreen. Allow acne medication to dry b...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl peroxide 2.5%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

Treats and helps prevent new acne blemishes.

Warnings

WARNINGS SECTION

For external use only.

Do not use if you have

OTC - DO NOT USE SECTION

very sensitive skin or if you are sensitive to benzoyl peroxide.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation becomes severe and continues.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

When using this product

OTC - WHEN USING SECTION

  • avoid unnecessary sun exposure and use a sunscreen
  • using other topical acne drugs at the same time or right after use may increase dryness or irritation of skin. If this occurs, only one drug should be used.
  • keep away from eyes, lips, mouth
  • this product may bleach hair or dyed fabrics

Directions

DOSAGE & ADMINISTRATION SECTION

Cleanse skin thoroughly before applying. COver entire affected area with a thin layer 1 to 3 times daily. Start with one application daily, because excessive drying may occur. Then gradually increase to 2 to 3 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 outsie use a sunscreen. Allow acne medication to dry before application of sunscreen. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Other information

OTHER SAFETY INFORMATION

  • Keep tightly closed
  • Avoid storing at extreme temperatures (below 40 F and above 100 F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Bentonite, Caprylic/Capric Triglyceride, Glycerin, Emulsifying Wax NF, Polysorbate 20, Glyceryl Laurate, Cetyl Dimethicone, Magnesium Aluminum Silicate, Xanthan Gum, Sodium Citrate, Disodium EDTA, Citric Acid, Methylparaben, Propylparaben.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
200009benzoyl peroxide 2.5 % Topical LotionPSN2
200009benzoyl peroxide 25 MG/ML Topical LotionSCD2
200009benzoyl peroxide 2.5 % Topical LotionSY2

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
69842-181-012020-01-31C16284748780-19d75b9d0-3d5d-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-181-01Targeted Acne Spot TreatmentCVS1 in 1 CARTONLOTION12
69842-181-01Targeted Acne Spot TreatmentCVS21 g in 1 TUBELOTION212

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-181TARGETED ACNE SPOT TREATMENT CVS (BENZOYL PEROXIDE 2.50%) LOTION [CVS]2Legacy NDC, 2 package rows20180226_e7dee980-efab-4c38-b29a-8e5fbf65afa6.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-18169842-181-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
23da5c40-4309-448d-9ac3-5d77da4deb03e7dee980-efab-4c38-b29a-8e5fbf65afa62018-02-26WarningsExact identifier
spl id: 23da5c40-4309-448d-9ac3-5d77da4deb03
spl set id: e7dee980-efab-4c38-b29a-8e5fbf65afa6

Reported adverse events (FAERS/openFDA)#

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