FDA.reportPublic FDA data

Proactivplus Pore Clearing Treatment

Manufacturer
Alchemee, LLC | VEE PAK, LLC
Effective date
2026-08-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-09-03 03:03:26

Label at a glance#

ProductProactivplus Pore Clearing Treatment
Active ingredientSALICYLIC ACID
Label structure13 sections

Dosage and administration

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 below. 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 ...

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

  • 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.
  • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

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 days. If no discomfort occurs, follow the directions stated below.
  • 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.

Other Information

OTHER SAFETY INFORMATION

Store at 20 - 25°C (68 - 77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua/Eau), Glycerin, Ethylhexyl Palmitate, Polyacrylamide, Ethoxydiglycol, Cetearyl Alcohol, PEG-120 Methyl Glucose Dioleate, Aluminum Starch Octenylsuccinate, C13-14 Isoparaffin, Cetyl Alcohol, Phenoxyethanol, Parfum (Fragrance), Polysorbate 20, Dimethicone, Sodium Hydroxide, Xanthan Gum, Laureth-7, Aloe Barbadensis Leaf Juice, Chlorphenesin, Benzoic Acid, Butylene Glycol, Dipotassium Glycyrrhizate, Sorbic Acid, Lonicera Japonica (Honeysuckle) Flower Extract, Tocopherol, Potassium Sorbate, Sodium Benzoate, Citric Acid, Alpha-Isomethyl Ionone, Citronellol, Geraniol, Hexyl Cinnamal, Hydroxycitronellal, Linalool, Tetramethyl Acetyloctahydronaphthalenes

Questions or comments?

OTC - QUESTIONS SECTION

1-800-309-4796

Distributed by

SPL UNCLASSIFIED SECTION

Distributed by Alchemee LLC
Hawthorne, NY 10532
Made in the USA of Foreign
and Domestic Components
Questions? 1-800-309-4796 • proactiv.com

Proactiv is a registered trademark
of Taro Pharmaceuticals U.S.A., Inc.

PRINCIPAL DISPLAY PANEL - 89 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

proactiv+

Pore

Clearing

Treatment

acne medication

2% salicylic acid

Step 2

3 Fl. Oz. (89 ml)

image 1image 1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 36 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11410-04711410-047-30, 11410-047-90

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
BENZYL BENZOATEN863NB338GIACT
.DELTA.-TOCOPHEROLJU84X1II0NIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
HEXYL CINNAMAL7X6O37OK2IIACT
SODIUM BENZOATEOJ245FE5EUIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
CETEARYL ALCOHOL2DMT128M1SIACT
LONICERA JAPONICA FLOWER4465L2WS4YIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
CITRALT7EU0O9VPPIACT
ETHYLHEXYL PALMITATE2865993309IACT
POLYACRYLAMIDE (CROSSLINKED; 2 MOLE PERCENT BISACRYLAMIDE)9FPL31B58QIACT
DIPOTASSIUM GLYCYRRHIZATECA2Y0FE3FXIACT
GERANIOLL837108USYIACT
LAURETH-7Z95S6G8201IACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
LINALOOLD81QY6I88EIACT
CITRIC ACID2968PHW8QPIACT
DIMETHICONE92RU3N3Y1OIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
CHLORPHENESINI670DAL4SZIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
XANTHAN GUMTTV12P4NEEIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM HYDROXIDE55X04QC32IIACT
CETYL ALCOHOL936JST6JCNIACT
POLYSORBATE 207T1F30V5YHIACT
CITRONELLOLP01OUT964KIACT
DIETHYLENE GLYCOL MONOETHYL ETHERA1A1I8X02BIACT
SORBIC ACIDX045WJ989BIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
BENZOIC ACID8SKN0B0MIMIACT
BUTYLENE GLYCOL3XUS85K0RAIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32026-01-07full-release2026-06-01 01:31:41

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
Proactivplus Pore Clearing TreatmentSALICYLIC ACIDAlchemee, LLC334efe89-3775-5ddb-e063-6294a90ae3a82026-08-27WarningsExact identifier
ndc (package): 11410-047-30
ndc (package): 11410-047-90
ndc (product): 11410-047
ndc11 (package): 11410004790
ndc11 (package): 11410004730
spl id: 5a0c0274-8d95-a8e6-e063-6394a90a6d2f
spl set id: 334efe89-3775-5ddb-e063-6294a90ae3a8

Reported adverse events (FAERS/openFDA)#

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