ACNE BANISHING BODY- salicylic acid spray

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredients

Salicylic Acid (2.0%)

Purpose

Acne treatment

Use

For the treatment of acne

Warnings

For external use only

Flammable

Avoid Spraying in eyes

Content under pressure

Do not use

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

When using this product

• 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.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• 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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACNE BANISHING BODY 
salicylic acid spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72667-218
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ALOE (UNII: V5VD430YW9)
WATER (UNII: 059QF0KO0R)
BENZOIC ACID (UNII: 8SKN0B0MIM)
BENZYL ALCOHOL (UNII: LKG8494WBH)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
GLYCERIN (UNII: PDC6A3C0OX)
HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER (UNII: 8FP93ED6H2)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
NIACINAMIDE (UNII: 25X51I8RD4)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
SORBIC ACID (UNII: X045WJ989B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72667-218-06	170 g in 1 CAN; Type 0: Not a Combination Product	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	12/01/2025

Labeler - Inspec Solutions (081030372)

Registrant - Inspec Solutions (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions		081030372	manufacture(72667-218)