FDA.reportPublic FDA data

Panoxyl Acne Banishing Body Spray

Manufacturer
Inspec Solutions
Effective date
2026-04-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:53:29

Label at a glance#

ProductAcne Banishing Body
Active ingredientSALICYLIC ACID
Label structure7 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.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid (2.0%)

Purpose

OTC - PURPOSE SECTION

Acne treatment

Use

INDICATIONS & USAGE SECTION

For the treatment of acne

Warnings

WARNINGS SECTION

For external use only

Flammable

Avoid Spraying in eyes

Content under pressure

Do not use

OTC - DO NOT USE SECTION

  • In or near eyes. If contact occurs, flush thoroughly with water.
  • If irritation or redness develops, discontinue use.

When using this product

OTC - WHEN USING SECTION

  • Apply to affected areas only.
  • 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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.

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1048903salicylic acid 2 % Topical SprayPSN2
1048903salicylic acid 20 MG/ML Topical SpraySCD2
1048903salicylic acid 2 % Topical SpraySY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72667-218-06Acne Banishing Body170 g in 1 CANSPRAY1702

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
72667-21872667-218-06

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
ALCOHOL3K9958V90MIACT
ALOEV5VD430YW9IACT
WATER059QF0KO0RIACT
BENZOIC ACID8SKN0B0MIMIACT
BENZYL ALCOHOLLKG8494WBHIACT
DIPROPYLENE GLYCOLE107L85C40IACT
GLUCONOLACTONEWQ29KQ9POTIACT
GLYCERINPDC6A3C0OXIACT
HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER8FP93ED6H2IACT
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATED2QHA03458IACT
NIACINAMIDE25X51I8RD4IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM ASCORBYL PHOSPHATE836SJG51DRIACT
SORBIC ACIDX045WJ989BIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
594474b1-4559-b936-e063-6394a90a87ca10f9e67f-ec10-4237-bd4d-24cb594c37892026-08-17WarningsExact identifier
spl set id: 10f9e67f-ec10-4237-bd4d-24cb594c3789

Reported adverse events (FAERS/openFDA)#

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