Salicylic Acid

Manufacturer
The Center Brands, LLC | DIMENSIONAL MERCHANDISING INC
Effective date
2022-06-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:57:16

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure10 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION


Directions
• 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 and ask a doctor.

INDICATIONS & USAGE SECTION


Directions
• 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 and ask a doctor.

OTC - ACTIVE INGREDIENT SECTION


Purpose
Salicylic Acid 2.00%..............................................Acne Treatment

OTC - PURPOSE SECTION


Uses
• Helps fight existing acne breakouts and prevents future acne
breakouts.

WARNINGS SECTION


Warnings
For external use only.
When using this product skin irritation and dryness are more
likely to occur when using another topical acne product at the
same time.
If irritation occurs, use only one acne product at a time.
Avoid eye area. In case of eye contact, flush gently and
thoroughly with water. Do not apply to broken or irritated skin.
Keep out of reach of children.

OTC - DO NOT USE SECTION


If irritation occurs, use only one acne product at a time.
Avoid eye area. In case of eye contact, flush gently and
thoroughly with water. Do not apply to broken or irritated skin.

OTHER SAFETY INFORMATION


Other Information
Sensitivity Test for a New User. Apply product sparingly to one or
two small affected areas during the first 3 days. If no discomfort
occurs, follow the directions stated above. Store in controlled
temperatures (4-20°C/39-68°F). Keep in a dark and dry place.
Keep container tightly closed.

INACTIVE INGREDIENT SECTION


Inactive Ingredients
Aqua (Water), Propanediol, Sodium Polyacrylate, Maltobionic Acid,
Amorphophallus Konjac Root Extract, Caprylyl Glycol,
Phenoxyethanol, Carbomer, Dipropylene Glycol, Sodium Phytate,
Sodium Hydroxide, Xanthan Gum.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82800-00382800-003-01

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0a5dc604-736d-d8c3-e063-6294a90a3251e37b661f-071b-5c73-e053-2995a90a318e2023-11-17WarningsExact identifier
spl set id: e37b661f-071b-5c73-e053-2995a90a318e

Reported adverse events (FAERS/openFDA)#

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