ACNE BODY WASH- salicylic acid soap

Acne Body Wash by

Drug Labeling and Warnings

Acne Body Wash by is a Otc medication manufactured, distributed, or labeled by Curology. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic Acid 2%

Purpose

Acne treatment

Uses

For the treatment of acne

Warnings

For external use only

When using this product

• 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.

Keep out of reach of children.

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

Directions

• Dampen skin and massage a thin layer onto the entire affected area then rinse thoroughly.
• 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

Store at 20°-25°C (68°-77°F)

Inactive Ingredients

Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Cocamidopropyl Betaine, Cocamidopropyl Dimethylamine, Polygiyceryl-4 Caprate, Polyglyceryl-6 Caprylate, Hydroxypropyl Methylcellulose, Phenoxyethanol, Sodium Chloride, Zinc Pyrithione, Sodium Hydroxide, Polyquaternium-7, Ethylhexylglycerin, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Disodium EDTA, Sodium Benzoate

Questions?

858-859-1188

Principal Display Panel – 100 mL Tube Label

Curology

Acne Body Wash

2% Salicylic Acid Acne Treatment
with clarifying tea tree oil

DERMATOLOGIST
FOUNDEDDEVELOPEDTESTED

100 ml/3.4 fl oz

INGREDIENTS AND APPEARANCE

ACNE BODY WASH 
salicylic acid soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82575-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Glycerin (UNII: PDC6A3C0OX)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Cocamidopropyl Dimethylamine (UNII: L36BM7DG2T)
Hypromellose, Unspecified (UNII: 3NXW29V3WO)
Polyglyceryl-4 Caprate (UNII: 3N873UN885)
Polyglyceryl-6 Caprylate (UNII: DGV8R54VG7)
Phenoxyethanol (UNII: HIE492ZZ3T)
Pyrithione Zinc (UNII: R953O2RHZ5)
Polyquaternium-7 (70/30 Acrylamide/Dadmac; 1600000 MW) (UNII: 0L414VCS5Y)
Ethylhexylglycerin (UNII: 147D247K3P)
Sodium Hydroxide (UNII: 55X04QC32I)
Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM)
Tea Tree Oil (UNII: VIF565UC2G)
Sodium Chloride (UNII: 451W47IQ8X)
Edetic Acid (UNII: 9G34HU7RV0)
Sodium Benzoate (UNII: OJ245FE5EU)
Formaldehyde/Sodium Naphthalenesulfonate Copolymer (3000 MW) (UNII: 90D834OZUI)
Xanthan Gum (UNII: TTV12P4NEE)
Magnesium Nitrate (UNII: 77CBG3UN78)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Magnesium Chloride (UNII: 02F3473H9O)
Methylisothiazolinone (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82575-110-30	267 mL in 1 TUBE; Type 0: Not a Combination Product	12/01/2023
2	NDC: 82575-110-40	100 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2024
3	NDC: 82575-110-50	200 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	12/01/2023

Labeler - Curology (104103284)