Paulas Choice Clear Daily Skin Clearing Treatment

Manufacturer
Paula's Choice
Effective date
2022-12-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:42:14

Label at a glance#

ProductPaulas Choice Clear Daily Skin Clearing Treatment
Active ingredientBENZOYL PEROXIDE
Label structure13 sections

Label contents#

Full prescribing information#

OTC - PREGNANCY OR BREAST FEEDING SECTION

For the treatment of Acne

Penetrates pores to control acne blemishes, blackheads and whiteheads.

Helps prevent new acne blemishes, blackheads and whiteheads.

WARNINGS SECTION

For external use only.

Do not use if you:

- Have very sensitive skin

-Are sensitive to benzoyl peroxide.

OTC - WHEN USING SECTION

- Skin irritation and dryness is more likely to occur if you use another topical medication at the same time.

-If irritation occurs, only use one topical acne medication at a time

-Avoid unnecessary sun expossure

-Avoid contact with the eyes, lip 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, peling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

OTC - STOP USE SECTION

Stop use and ask doctor if skin irritation occurs or get worse.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INSTRUCTIONS FOR USE SECTION

Apply after cleansing and exfoliating.

Cover the entire affected area with a thin layer one to three times daily

Because excessive drying of the skin may occur, start wit oe 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, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

OTHER SAFETY INFORMATION

Store at 20-25 degrees Celcius.

INACTIVE INGREDIENT SECTION

Water (Aqua), Propylene Glycol, Bisabolol, Allantoin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Hydroxyethylcellulose, Sodium Citrate, Laureth-4, Caprylyl Glycol, Sodium Hydroxide, Disodium EDTA, Hexylene Glycol, Phenoxyethanol.

OTC - ACTIVE INGREDIENT SECTION

Benzoyl Peroxide, 2.5%

OTC - PURPOSE SECTION

For the treatment of acne. Penetrates pores to control acne blemishes, blackheads and whiteheads. Helps prevent new acne blemishesm blackheads and whiteheads.

INDICATIONS & USAGE SECTION

- Apply after cleansing and exfoliating

-Cover the entir eaffected area with a thin layer one to three times daily

-Becase 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, appy sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

DOSAGE & ADMINISTRATION SECTION

Benzoyl Peroxide, 2.5%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

6100 Component6100 Component

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76144-61076144-610-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f08ade83-92b3-3035-e053-2995a90a78ecf08ade83-92b2-3035-e053-2995a90a78ec2022-12-23WarningsExact identifier
spl id: f08ade83-92b3-3035-e053-2995a90a78ec
spl set id: f08ade83-92b2-3035-e053-2995a90a78ec

Reported adverse events (FAERS/openFDA)#

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