FDA.reportPublic FDA data

PanOxyl Acne Gel Wash

Manufacturer
Crown Laboratories, Inc.
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:32:29

Label at a glance#

ProductPanOxyl Acne Gel Wash
Active ingredientSALICYLIC ACID
Label structure9 sections

Dosage and administration

wet face and work product into a lather cover the entire affected area with a thin layer in the morning and at night rinse thoroughly and pat dry 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 day

Storage and handling

Store at 20 o - 25 o C (68 o - 77 o F) [see USP Controlled Room Temperature].

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

Acne Medication

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.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

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

  • wet face and work product into a lather
  • cover the entire affected area with a thin layer in the morning and at night
  • rinse thoroughly and pat dry
  • 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 day

Other information

STORAGE AND HANDLING SECTION

  • Store at 20 o - 25 oC (68 o - 77 oF) [see USP Controlled Room Temperature].

Inactive ingredients

INACTIVE INGREDIENT SECTION

1,2-Hexanediol, Allantoin, Aloe Barbadensis Leaf Juice, Aqua, Betaine, Camellia Sinensis Leaf Extract, Caprylyl Glycol, Citric Acid, Cocamidopropyl Hydroxysultaine, Decyl Glucoside, Glycerin, PEG-150 Distearate, Potassium Sorbate, Saccharide Isomerate, Sodium Benzoate, Sodium C14-16 Olefin Sulfonate, Sodium Chloride, Sodium Citrate, Sodium Hydroxide, Spirulina Platensis Extract, Zinc PCA

Questions?

OTC - QUESTIONS SECTION

call 1-833-279-6522

PanOxyl Acne Gel Wash Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW

PanOxyl

Acne Gel Wash

for Face

2% SALICYLIC ACID

ACNE TREATMENT WASH

Clears and helps prevent acne

Gentle gel-to-foam formula

Zinc PCA helps target excess oil

DERMATOLIGST RECOMMENDED

6.5 fl oz (192ml)

Distributed by: Crown Laboratories, Inc.

Johnson City, TN 37604

P12717.00

PanOxyl Acne Gel Wash labelPanOxyl Acne Gel Wash label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
562600salicylic acid 2 % Medicated Liquid SoapPSN2
562600salicylic acid 20 MG/ML Medicated Liquid SoapSCD2
562600salicylic acid 2 % Facial Cleanser TonerSY2
562600salicylic acid 2 % Facial ScrubSY2
562600salicylic acid 2 % Medicated Liquid SoapSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0316-0299-01PanOxyl Acne Gel Wash192 mL in 1 BOTTLE, PUMPGEL1922
0316-0299-03PanOxyl Acne Gel Wash89 mL in 1 BOTTLE, PUMPGEL892

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0316-0299-01ML - Milliliter0316-02996bb31c8f-a23d-47c3-bc53-539af19a4faf12025-11-13
0316-0299-03ML - Milliliter0316-0299bea344db-bb83-4125-8525-9fc5e47eb28012025-11-13

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0316-02990316-0299-01, 0316-0299-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
1,2-HEXANEDIOLTR046Y3K1GIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CAPRYLYL GLYCOL00YIU5438UIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
SACCHARIDE ISOMERATEW8K377W98IIACT
SODIUM CITRATE1Q73Q2JULRIACT
SALICYLIC ACIDO414PZ4LPZACTIB
GLYCERINPDC6A3C0OXIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
BETAINE3SCV180C9WIACT
CITRIC ACID2968PHW8QPIACT
SODIUM CHLORIDE451W47IQ8XIACT
SPIRULINA PLATENSIS9L3TIH1UUEIACT
WATER059QF0KO0RIACT
SODIUM BENZOATEOJ245FE5EUIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
SODIUM HYDROXIDE55X04QC32IIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
ZINC PCAC32PQ86DH4IACT
ALLANTOIN344S277G0ZIACT

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
PanOxyl Acne Gel WashSALICYLIC ACIDCrown Laboratories, Inc.39712bb8-3d4e-29b3-e063-6394a90a95b82026-01-12WarningsExact identifier
ndc (package): 0316-0299-01
ndc (package): 0316-0299-03
ndc (product): 0316-0299
ndc11 (package): 00316029903
ndc11 (package): 00316029901
spl id: 48344cd1-d22c-7c9f-e063-6394a90af908
spl set id: 39712bb8-3d4e-29b3-e063-6394a90a95b8

Reported adverse events (FAERS/openFDA)#

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