AcneFree Dermatology Inspired Care Sensitive Skin 24 Hr Acne Clearing System

Manufacturer
L'Oreal USA Products Inc | Universal Packaging Systems, Inc. (DBA: PakLab)
Effective date
2021-07-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:41:14

Label at a glance#

ProductAcneFree Dermatology Inspired Care Sensitive Skin 24 Hr Acne Clearing System
Active ingredientBENZOYL PEROXIDE, SALICYLIC ACID
Label structure30 sections

Dosage and administration

clean the skin thoroughly before applying this product cover the entire affected area with a thin layer one to three times daily 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, apply ...

Storage and handling

Store at 60°-95° F (15°-35° C)

Label contents#

Full prescribing information#

Sensitive Skin Acne Lotion

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl peroxide 3%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Use

INDICATIONS & USAGE SECTION

for the treatment of acne

Warnings

WARNINGS SECTION

For external use only

Do not use if you

OTC - DO NOT USE SECTION

  • have very sensitive skin
  • are sensitive to benzoyl peroxide

When using this product

OTC - WHEN USING SECTION

  • skin irritation and dryness is more liekly 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.
  • 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 irritaiton 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

OTC - STOP USE SECTION

skin irritation becomes severe

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the skin thoroughly before applying this product
  • cover the entire affected area with a thin layer one to three times daily
  • 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, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both producs and ask a doctor.

Other information

STORAGE AND HANDLING SECTION

Store at 60°-95° F (15°-35° C)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Ethyl Macadamiate, Propanediol, Glycerin, Butylene Glycol, Polyacrylamide, Phenoxyethanol, C13-14 Isoparaffin, Bisabolol, Laureth-7, Allantoin, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methylisothiazolinone, Sodium Hyaluronate, Methyl Methacrylate/Glycol Dimethacrylate Crosspolymer, Sodium Hydroxide, Sea Whip Extract, Zingiber Officinale (Ginger) Root Extract

Questions or comments?

OTC - QUESTIONS SECTION

1-888-768-2913

Salicylic Acid Acne Cleanser

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 1.5%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Use

INDICATIONS & USAGE SECTION

for the treatment of acne

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

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.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • use every morning and evening
  • apply a dime-size amount to damp skin and gently massage, avoiding the eye area
  • rinse well
  • if bothersome dryness or peeling occurs, reduce application use
  • may be used on chest or back

Other information

STORAGE AND HANDLING SECTION

store at 60°-95° F (15°-35° C)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Cocoyl Isethionate, Stearic Acid, Cocamidopropyl Betaine, Sodium Lauroamphoacetate, Disodium Laureth Sulfosuccinate, Glycol Distearate, Polyacrylate-1 Crosspolymer, Benzyl Alcohol, Avena Sativa (Oat) Kernel Extract, Sodium Phytate, Zinc PCA, Glycerin, Sorbic Acid, Ethyl Vanillin, Butylene Glycol, Sea Whip Extract, Aminomethyl Propanol

Questions or comments?

OTC - QUESTIONS SECTION

1-888-768-2913

Directions

INDICATIONS & USAGE SECTION

Use every morning and evening. After cleansing, apply to entire face with a cotton pad, avoiding the eye area. Do not rinse. May also be used on chest or back.

Ingredients

INACTIVE INGREDIENT SECTION

Water, Niacinamide, Camellia Sinensis Leaf Extract, Pyrus Malus (Apple) Fruit Extract, Citrus Aurantium Dulcis (Orange) Fruit Extract, Citrus Medica Limonum (Lemon) Extract, Sea Whip Extract, Saccharum Officinarum (Sugar Cane) Extract, Zingiber Officinale (Ginger) Root Extract, Pentylene Glycol, Benzyl Alcohol, Isoceteth-20, Aminomethyl Propanol, Salicylic Acid, Disodium EDTA, Bisabolol, Benzalkonium Chloride, Glycerin, Sorbic Acid, Butylene Glycol

Questions or comments?

OTC - QUESTIONS SECTION

1-888-768-2913

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-03449967-034-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 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
5edf8299-0d09-4fb8-bc36-5b70b298a717fbb259a9-381f-4c2d-9a74-c85564294caf2021-07-15WarningsExact identifier
spl set id: fbb259a9-381f-4c2d-9a74-c85564294caf

Reported adverse events (FAERS/openFDA)#

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