Salicylic Acid

Manufacturer
The Center Brands | DIMENSIONAL MERCHANDISING INC
Effective date
2022-09-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:53:56

Label at a glance#

ProductSalicylic Acid
Active ingredientSALICYLIC ACID
Label structure11 sections

Label contents#

Full prescribing information#

Drug Facts Active

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 2%--------Acne Treatment

Drug Facts Purpose

OTC - PURPOSE SECTION

Salicylic acid 2%..........acne treatment

Warnings

WARNINGS SECTION

For external use only.

When using this product skin irritation and dryness are more likely to occue 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 contact, flush gently nd throroughly with water. Do not apply to broken or irrritated skin.

Keep out of reach of children. If swallowed, seek medical help.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, seek medical help.

OTC - STOP USE SECTION

When using this product skin irritation and dryness are more likely to occue 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 contact, flush gently nd throroughly with water. Do not apply to broken or irrritated skin.

INDICATIONS & USAGE SECTION

Shake well.

clean the skin thoroughly beforee 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 - ASK DOCTOR SECTION

if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use and ask a doctor.

OTHER SAFETY INFORMATION

Sensitivity test for a new user. Apply product sparingly to one or two small affected areas during the first three days. If no discomfort occurs, follow the directions started above. Store in controlled temperatures (4-20C/39-68F). Keep in a dark and dry place. Keep container tightly closed.

INACTIVE INGREDIENT SECTION

Aqua, Propenediol, Sodium Polyacrylate, Maltobionic Acid, Amorphophallus Konjac Root Extract, Caprylyl Glycol, Phenoxyethanol, Carbomer, Dipropylene Glycol, Sodium Phytate, Sodium Hydroxide, Xanthan Gum

DOSAGE & ADMINISTRATION SECTION

Shake well.

clean the skin thoroughly beforee 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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82800-00482800-004-01

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
0a5da177-7ab7-fb90-e063-6294a90a7d14e883274f-8357-4052-e053-2a95a90a288d2023-11-17WarningsExact identifier
spl set id: e883274f-8357-4052-e053-2a95a90a288d

Reported adverse events (FAERS/openFDA)#

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