Proactiv ® Skin Clearing Water Gel

Manufacturer
The Proactiv Company, LLC | KIK Holdco Company Inc
Effective date
2017-03-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:03:17

Label at a glance#

ProductProactiv Skin Clearing Water
Active ingredientSALICYLIC ACID
Label structure10 sections

Dosage and administration

Sensitivity Test for a New User: Apply product sparingly to one or two small affected areas during the first 3 uses. If no discomfort occurs, follow the directions stated below. cleanse 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 ...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 2%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Use

INDICATIONS & USAGE SECTION

for the management of acne

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not use this product more than three times per day.
  • skin irritation and dryness are 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.
  • avoid contact with eyes. If contact occurs rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • 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

  • Sensitivity Test for a New User: Apply product sparingly to one or two small affected areas during the first 3 uses. If no discomfort occurs, follow the directions stated below.
  • cleanse 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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Niacinamide, Cyclopentasiloxane, Dimethicone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Cetyl Ethylhexanoate, Dimethicone/Vinyl Dimethicone Crosspolymer, Silica, Propanediol, Polygonum Cuspidatum Root Extract, Myristyl Alcohol, Tetrasodium EDTA, PCA, Ethylhexylglycerin, Sodium Hyaluronate, Sodium Hydroxide, 1,2-Hexanediol, Caprylyl Glycol, Isohexadecane, Polysorbate 60, Phenoxyethanol, Fragrance, Blue 1

Questions or comments?

OTC - QUESTIONS SECTION

Within US 1-800-950-4695

SPL UNCLASSIFIED SECTION

Distributed by The Proactiv Company, LLC.
100 N Sepulveda Blvd., El Segundo, CA 90245

PRINCIPAL DISPLAY PANEL - 90mL Tube Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

proactiv®

SKIN CLEARING WATER GEL

3 FL. OZ. 90mL

salicylic acid acne medication

PRINCIPAL DISPLAY PANEL - 90 mL Tube Box
PRINCIPAL DISPLAY PANEL - 90 mL Tube Box

Products#

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DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11410-04911410-049-74, 11410-049-77

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 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
5ff71a46-a335-42d5-8176-714f9cacec593ca06ae5-3c23-4d4e-9635-c4a3d07d874a2022-12-19WarningsExact identifier
spl set id: 3ca06ae5-3c23-4d4e-9635-c4a3d07d874a

Reported adverse events (FAERS/openFDA)#

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