MAX COMPLEXION CORRECTION PADS- salicylic acid liquid

MAX COMPLEXION CORRECTION PADS by

Drug Labeling and Warnings

MAX COMPLEXION CORRECTION PADS by is a Otc medication manufactured, distributed, or labeled by PETER THOMAS ROTH LABS LLC, JUNE JACOBS LABS LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Salicylic Acid 2%

PURPOSE

PURPOSE

Acne Treatment

INDICATIONS & USAGE

USE

• For the treatement and management of acne .

WARNINGS

Warnings

For external use only.

WHEN USING

When using this product 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 medication at a time.

Avoid contact with eyes. If contact occurs, flush thoroughly with water

KEEP OUT OF REACH OF CHILDREN

Keep Out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

OTHER SAFETY INFORMATION

Flammable: Keep away from extreme heat or flame.

Avoid the eyes, lips., other mucous membranes and overdry or sensitive areas.

DOSAGE & ADMINISTRATION

Directions

• Cleanse skin thoroughly before applying this product.
• Gently wipe entire affected area with a thin layer one to three times a day.
• Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three times daily or as directed by a doctor.
• If bothersome dryness or peeling occurs, reduce application to once a day or everyother day.

INACTIVE INGREDIENT

Inactive Ingredients

Alcohol, Water/Aqua/Eau, Butylne glycol, Glycolic Acid, Hamamelis Virginiana (Witch Hazel) Water, Aloe Barbadensis Leaf Juice, Arginine, Sodium Hydroxide, Chamomilla Recutita (Matricaria) Flower Extract, Prunus Persia (Peach) Fruit Extract, Fragrance/Parfum, t-Butyl Alcohol, Camellia Sinensis Leaf Extract, Phenoxyethanol, Symphytum Officinale Root Extract, Denatonium Benzoate, Allantoin, Benzoic Acid, Potassium Sorbate, Citric Acid, Sodium Benzoate.

QUESTIONS

Questions or comments

Call toll free 1-800-PTR-SKIN (787-7546)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MAX COMPLEXION CORRECTION PADS 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54031-501
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 mL

Inactive Ingredients
Ingredient Name	Strength
2-T-BUTYLCYCLOHEXYL ACETATE (UNII: 364FV60913)
BENZYL ACETATE (UNII: 0ECG3V79ZJ)
IONONE (UNII: QP734LIN1K)
COMFREY ROOT (UNII: M9VVZ08EKQ)
WATER (UNII: 059QF0KO0R)
PRUNUS PERSICA (PEACH) FRUIT (UNII: 3OKE88I3QG)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
LINALOOL (UNII: D81QY6I88E)
CITRONELLOL (UNII: P01OUT964K)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CITRIC ACID (UNII: 2968PHW8QP)
CHAMOMILE (UNII: FGL3685T2X)
BENZOIC ACID (UNII: 8SKN0B0MIM)
AMYL CINNAMAL (UNII: WC51CA3418)
PHENETHYL ALCOHOL (UNII: ML9LGA7468)
ISOBUTYL METHYL TETRAHYDROPYRANOL (UNII: VK5ZHH2T3F)
DIMETHYL PHENETHYL BUTYRATE (UNII: 3Q0C60547R)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
ALLANTOIN (UNII: 344S277G0Z)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ARGININE (UNII: 94ZLA3W45F)
GAMMA-DECALACTONE (UNII: 7HLS05KP9O)
ALCOHOL (UNII: 3K9958V90M)
GLYCOLIC ACID (UNII: 0WT12SX38S)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
T-BUTYL ALCOHOL (UNII: MD83SFE959)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
GERANIOL (UNII: L837108USY)
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
ACETYL HEXAMETHYL TETRALIN (UNII: 360Q8Z01IP)
GAMMA-UNDECALACTONE (UNII: QB1T0AG2YL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54031-501-22	1 in 1 CARTON	03/25/2025
1		60 in 1 JAR
1		1 mL in 1 PATCH; 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	03/25/2025

Labeler - PETER THOMAS ROTH LABS LLC (780458944)

Registrant - JUNE JACOBS LABS LLC (122610681)

Establishment
Name	Address	ID/FEI	Business Operations
JUNE JACOBS LABS LLC		122610681	manufacture(54031-501)