PEACH SLICES 3 STEP ACNE STARTER KIT- salicylic acid kit

Peach Slices 3 Step Acne Starter Kit by

Drug Labeling and Warnings

Peach Slices 3 Step Acne Starter Kit by is a Otc medication manufactured, distributed, or labeled by Peach & Lily, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts:

Active ingredient 

Salicylic Acid 2%

Purpose

Acne medication

Use:

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

Sun Alert:

Because this product may make your skin more sensitive to the sun, be certain you have adequate sunscreen protection while using this product and for a week after you discontinue use.

Keep out of reach of children.

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

Directions:

• Wet face.
• Dispense product into hands and massage gently onto face and neck, avoiding the delicate eye area.
• Cover the entire affected area with a thin layer and rinse thoroughly with warm water 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:

Water (Aqua), Glycerin, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Betaine, Sodium Chloride, Cucumis Sativus (Cucumber) Fruit Water, Sodium Hyaluronate, Centella Asiatica Extract, Malpighia Emarginata (Acerola) Fruit Extract, Sodium Benzoate, Butylene Glycol, Potassium Sorbate, Caprylyl Glycol, 1,2-Hexanediol, Sodium Hydroxide, Citric Acid, Ethylhexylglycerin, Phenoxyethanol

Questions or Comments?

1-866-519-4752

Drug Facts:

Active ingredient

Salicylic Acid 2%

Purpose

Acne medication

Use:

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 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.

Sunburn Alert:

• This product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn.
• Use a sunscreen, wear protective clothing, and limit sun exposure while using this product and for a week afterward.

Keep out of reach of children.

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

Directions:

• Cleanse 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:

Water (Aqua), Butylene Glycol, Arginine, Allantoin, Cucumis Sativus (Cucumber) Fruit Water, Glycerin, Centella Asiatica Extract, Malpighia Emarginata (Acerola) Fruit Extract, Lactic Acid, Glycolic Acid, Potassium Sorbate, Sodium Benzoate, Citric Acid

Questions or Comments?

1-866-519-4752

Drug Facts:

Active ingredient

Salicylic Acid 0.5%

Purpose

Acne medication

Use:

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 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

Sun Alert:

Because this product may make your skin more sensitive to the sun, be certain you have adequate sunscreen protection while using this product and for a week after you discontinue use.

Keep out of reach of children.

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

Directions:

• Cleanse 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:

Water (Aqua), Caprylic/Capric Triglyceride, Propanediol, Butylene Glycol, Cetyl Ethylhexanoate, Ethoxydiglycol, Glyceryl Stearate, 1,2-Hexanediol, Cetearyl Alcohol, Cucumis Sativus (Cucumber) Fruit Water, Centella Asiatica Extract, Sodium Acetylated Hyaluronate, Sodium Hydrolyzed Crosspolymer, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate, Sclerotium Gum, Malpighia Emarginata (Acerola) Fruit Extract, Glycerin, Allantoin, Sodium Benzoate, Potassium Sorbate, Potassium Hydroxide, Sodium Phytate, Niacinamide, Polyacrylate Crosspolymer-6, Citric Acid, Ethylhexylglycerin, T-Butyl Alcohol, Pentylene GLycol, Sodium Polyacrylate

Questions or Comments?

1-866-519-4752

Package Labelling: Kit (

81515-540-00)

Package Labelling: 81515-541-01

Package Labelling: 81515-542-01

Package Labelling: 81515-543-01

INGREDIENTS AND APPEARANCE

PEACH SLICES 3 STEP ACNE STARTER KIT 
salicylic acid kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81515-540

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81515-540-00	1 in 1 KIT	08/14/2024

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 TUBE	30 mL
Part 2	1 BOTTLE	30 mL
Part 3	1 TUBE	30 mL

Part 1 of 3

ACNE CLARIFYING CLEANSER SALICYLIC ACID ACNE TREATMENT SULFATE FREE 
salicylic acid gel

Product Information
Item Code (Source)	NDC: 81515-541
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)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
BETAINE (UNII: 3SCV180C9W)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CUCUMBER FRUIT OIL (UNII: R81Y52NPCT)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
ACEROLA (UNII: XDD2WEC9L5)
SODIUM BENZOATE (UNII: OJ245FE5EU)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81515-541-01	1 in 1 CARTON
1		30 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	08/14/2024

Part 2 of 3

ACNE EXFOLIATING TONER SALICYLIC ACID ACNE TREATMENT ALCOHOL FREE 
salicylic acid solution

Product Information
Item Code (Source)	NDC: 81515-542
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)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ARGININE (UNII: 94ZLA3W45F)
ALLANTOIN (UNII: 344S277G0Z)
CUCUMBER FRUIT OIL (UNII: R81Y52NPCT)
GLYCERIN (UNII: PDC6A3C0OX)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
ACEROLA (UNII: XDD2WEC9L5)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
GLYCOLIC ACID (UNII: 0WT12SX38S)
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: 81515-542-01	1 in 1 CARTON
1		30 mL in 1 BOTTLE; 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	08/14/2024

Part 3 of 3

ACNE OIL FREE MOISTURIZER SALICYLIC ACID ACNE TREATMENT SILICONE FREE 
salicylic acid cream

Product Information
Item Code (Source)	NDC: 81515-543
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
PROPANEDIOL (UNII: 5965N8W85T)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CUCUMBER FRUIT OIL (UNII: R81Y52NPCT)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BETASIZOFIRAN (UNII: 2X51AD1X3T)
ACEROLA (UNII: XDD2WEC9L5)
GLYCERIN (UNII: PDC6A3C0OX)
ALLANTOIN (UNII: 344S277G0Z)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
PHYTATE SODIUM (UNII: 88496G1ERL)
NIACINAMIDE (UNII: 25X51I8RD4)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
PENTYLENE GLYCOL (UNII: 50C1307PZG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81515-543-01	1 in 1 CARTON
1		30 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	08/14/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	08/14/2024

Labeler - Peach & Lily, Inc (079906552)