OLOGY ACNE SPOT- salicylic acid gel

Ology Acne Spot by

Drug Labeling and Warnings

Ology Acne Spot by is a Otc medication manufactured, distributed, or labeled by Walgreens Co., Filltech USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Salicylic Acid 1.8%

Purpose

Acne Medication

Uses

• For the treatment of acne blemishes, acne pimples, blackheads, and whiteheads and allows skin to heal.

Warnings

For external use only.

When using this product

skin irritation or dryness may occur, especially if used with other topical acne medication. If it occurs, use only one ance treatment at a time, and reduce usage to every other day.

KEEP OUT OF REACH OF CHILDREN.

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

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. 

Other information

• Avoid storing at extreme temperatures (Below 40ºF and above 100ºF).

Inactive ingredients

Aqua (Water), 1,3 Propanediol, Glycerin, Azelaic Acid, Caprylyl Glycol, Aloe Barbadensis Leaf Juice, Polyacrylate Crosspolymer-6, Gaultheria Procumbens (Wintergreen) Leaf Extract, Ethylhexylglycerin, Sodium Hydroxide, Dipotassium Glycyrrhizate, Spiraea Ulmaria Flower Extract, Zinc PCA, Salix Alba (willow) Bark Extract, Sambucus Nigra Fruit Juice, 2-Methlpropan-2-ol, Potassium Sorbate, Sodium Benzoate, Citric Acid

Package Labeling:

INGREDIENTS AND APPEARANCE

OLOGY ACNE SPOT 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-9658
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	18 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPANEDIOL (UNII: 5965N8W85T)
GLYCERIN (UNII: PDC6A3C0OX)
AZELAIC ACID (UNII: F2VW3D43YT)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
GAULTHERIA PROCUMBENS LEAF (UNII: 2125M16OWN)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)
FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6)
ZINC PIDOLATE (UNII: C32PQ86DH4)
SALIX ALBA BARK (UNII: 205MXS71H7)
EUROPEAN ELDERBERRY JUICE (UNII: Z4IFJ0AK1E)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-9658-10	1 in 1 CARTON	07/16/2025
1		10 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	07/16/2025

Labeler - Walgreens Co. (008965063)

Registrant - Filltech USA, LLC (926433855)