FDA.reportPublic FDA data

PanOxyl Acne Banishing Body (Spray)

Manufacturer
Crown Laboratories, Inc.
Effective date
2026-01-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:31:26

Label at a glance#

ProductPanOxyl Acne Banishing Body (Spray)
Active ingredientSALICYLIC ACID
Label structure9 sections

Dosage and administration

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

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

Avoid spraying in eyes

Flammable: Keep away from fire or flame

Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F.

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

  • 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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denat., Aloe Barbadensis Leaf Extract, Aqua, Benzoic Acid, Benzyl Alcohol, Dipropylene Glycol, Gluconolactone, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Leuconostoc/Radish Root Ferment Filtrate, Niacinamide, Propylene Glycol, Sodium Ascorbyl Phosphate, Sorbic Acid

Questions?

OTC - QUESTIONS SECTION

call 1-833-279-6522

PanOxyl Acne Banishing Body Spray

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW

PanOxyl

Acne Banishing Body Spray

for Acne Prone Skin

2% SALICYLIC ACID

ACNE TREATMENT SPRAY

Clears blemishes and helps prevent future breakouts

Contains brightening Niacinamide and Vitamin C

Leave-on formula dries quickly

DERMATOLIGST RECOMMENDED

Net wt. 6oz (170g)

Distributed by: Crown Laboratories, Inc.

Johnson City, TN 37604

P12602.00

panoxyl.com

PanOxyl Acne Banishing Body Spray CanisterPanOxyl Acne Banishing Body Spray Canister

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1048903salicylic acid 2 % Topical SprayPSN3
1048903salicylic acid 20 MG/ML Topical SpraySCD3
1048903salicylic acid 2 % Topical SpraySY3

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
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0316-0297-01PanOxyl Acne Banishing Body (Spray)170 g in 1 CANISTERAEROSOL, SPRAY1703

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0316-0297-01GM - Gram0316-02976d76a5e8-980d-4107-a199-a3adbf76500412025-05-14

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0316-02970316-0297-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATED2QHA03458IACT
GLUCONOLACTONEWQ29KQ9POTIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SALICYLIC ACIDO414PZ4LPZACTIB
WATER059QF0KO0RIACT
HAMAMELIS VIRGINIANA TOP WATERNT00Y05A2VIACT
NIACINAMIDE25X51I8RD4IACT
ALCOHOL3K9958V90MIACT
GLYCERINPDC6A3C0OXIACT
DIPROPYLENE GLYCOLE107L85C40IACT
BENZOIC ACID8SKN0B0MIMIACT
SODIUM ASCORBYL PHOSPHATE836SJG51DRIACT
SORBIC ACIDX045WJ989BIACT
ALOE VERA LEAFZY81Z83H0XIACT
BENZYL ALCOHOLLKG8494WBHIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-11-12monthly-update2026-06-03 17:39:52
12024-09-26full-release2026-06-01 00:22:02

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 Banishing Body (Spray)SALICYLIC ACIDCrown Laboratories, Inc.2305f297-665d-e55f-e063-6394a90aa14e2026-01-05WarningsExact identifier
ndc (package): 0316-0297-01
ndc (product): 0316-0297
ndc11 (package): 00316029701
spl id: 47aa1bb3-0add-2167-e063-6294a90afeb4
spl set id: 2305f297-665d-e55f-e063-6394a90aa14e

Reported adverse events (FAERS/openFDA)#

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