Search by Drug Name or NDC

NDC 69842-0082-01 SkinPharmacy Advanced Acne Therapy Kit Details

SkinPharmacy Advanced Acne Therapy Kit

SkinPharmacy Advanced Acne Therapy Kit is a TOPICAL KIT in the HUMAN OTC DRUG category. It is labeled and distributed by CVS Health. The primary component is .

MedlinePlus Drug Summary

Benzoyl peroxide is used to treat mild to moderate acne.

Related Packages: 69842-0082-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Benzoyl Peroxide Topical

Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or birthmarks. Salicylic acid is in a class of medications called keratolytic agents. Topical salicylic acid treats acne by reducing swelling and redness and unplugging blocked skin pores to allow pimples to shrink. It treats other skin conditions by softening and loosening dry, scaly, or thickened skin so that it falls off or can be removed easily.

Related Packages: 69842-0082-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Salicylic Acid Topical

Product Information

NDC	69842-0082
Product ID	69842-082_80cecb53-6a09-4802-95fd-8d4130be8aa7
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	SkinPharmacy Advanced Acne Therapy Kit
Proprietary Name Suffix	n/a
Non-Proprietary Name	salicylic acid, benzoyl peroxide
Product Type	HUMAN OTC DRUG
Dosage Form	KIT
Route	TOPICAL
Active Ingredient Strength	n/a
Active Ingredient Units	n/a
Substance Name	n/a
Labeler Name	CVS Health
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part333D
Listing Certified Through	2024-12-31

Package

Package Images

NDC 69842-0082-01 (69842008201)

Pricing Information	N/A
NDC Package Code	69842-082-01
Billing NDC	69842008201
Package	1 KIT in 1 CARTON (69842-082-01) * 22 mL in 1 TUBE * 12 mL in 1 TUBE * 118 mL in 1 TUBE
Marketing Start Date	2014-10-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL a8c8cde4-c2bf-42aa-a3d1-a1846732e5e2 Details

SPL UNCLASSIFIED SECTION

4 FL OZ (118 mL)

Drug Facts

Active Ingredient

2% Salicylic Acid

Purpose

Acne Treatment

Use

For the management of acne

Warnings

For external use only

Ask a doctor or pharmacist before use if you are

Using other topical acne medications at the same time or immediately following use of this product. This may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

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 acne medication at a time.
When using this product avoid contact with eyes. If this occurs, immediately flush with water.

Keep out of reach of children. In case of accidental ingestion, get medical help or contact Poison Control Center right away.

Directions

Use morning and night.
Apply a dime sized amount to damp skin and gently massage for 1 to 2 minutes.
Rinse thoroughly with warm water.
Pat dry.
If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
If going outside use sunscreen

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Peg-8, Cocamidopropyl Betaine, Xanthan Gum, Lauryl Methacrylate/Glycol Dimethacrylate Crosspolymer, DMDM Hydantoin, Disodium EDTA, Tocopheryl Acetate, Hamamelis Virginiana (Witch Hazel) Water, Butylene Glycol, Sodium Benzotriazolyl Butylphenol Sulfonate, Calendula Officinalis Flower Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Phenoxyethanol, Yellow 5, Red 40, Fragrance.

SPL UNCLASSIFIED SECTION

ACTIVE CLEARING LOTION with Microsponge® Technology

0.75 FL OZ (22 mL)

Drug Facts

Active Ingredient

Benzoyl Peroxide 2.5%

Purpose

Acne Treatment

Use

for the management of acne

Warnings

For external use only

Do not use this medication if you

Have very sensitive skin
Are sensitive to benzoyl peroxide

When using this product

Avoid unnecessary sun exposure and use a sunscreen after using this product.
Avoid contact with lips, eyes, or mouth.
If product gets into eyes rinse thoroughly with water.
Skin irritation may occur, characterized by redness, burning, itching, peeling, or possible swelling. Irritation may be reduced by using the product less frequently or in lower concentration.
Avoid contact with hair and dyed fabrics, which may be bleached by this product.

Stop use and ask a doctor if irritation becomes severe.

Keep out of reach of children. Do not swallow. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Clean skin thoroughly before applying this product.
Apply a thin layer to affected area one to two times per day.
Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three time 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, Glycerin, Methyl Methacrylate/Glycol Dimethacrylate Crosspolymer, Cetyl Alcohol, Sorbitol, Glyceryl Dilaurate, Stearyl Alcohol, Magnesium Aluminum Silicate, Sodium Citrate, Silica, Sodium Lauryl Sulfate, Citric Acid, Methylparaben, Xanthan Gum, Propylparaben.

SPL UNCLASSIFIED SECTION

SPOT TREATMENT with Microsponge® Technology

0.4 FL OZ (12 mL)

Drug Facts

Active Ingredient

Benzoyl Peroxide 5%

Purpose

Acne Treatment

Use

for the management of acne

Warnings

For external use only

Do not use this medication if you

Have very sensitive skin
Are sensitive to benzoyl peroxide

When using this product

Avoid unnecessary sun exposure and use a sunscreen after using this product.
Avoid contact with lips, eyes, or mouth.
If product gets into eyes rinse thoroughly with water.
Skin irritation may occur, characterized by redness, burning, itching, peeling, or possible swelling. Irritation may be reduced by using the product less frequently or in lower concentration.
Avoid contact with hair and dyed fabrics, which may be bleached by this product.

Stop use and ask a doctor if irritation becomes severe.

Keep out of reach of children. Do not swallow. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Clean skin thoroughly before applying this product.
Cover the entire affected area with a thin layer one to three times daily.
If going outside apply sunscreen after using this product and consult a physician. Keep tightly closed and avoid storing at extreme temperatures (below 40°F and above 100°F).

Inactive ingredients

Water, Glycerin, Methyl Methacrylate/Glycol Dimethacrylate Crosspolymer, Sorbitol, Cetyl Alcohol, Glyceryl Dilaurate, Stearyl Alcohol, Magnesium Aluminum Silicate, Sodium Citrate, Silica, Sodium Lauryl Sulfate, Citric Acid, Methylparaben, Xanthan Gum, Propylparaben.

Distributed by: CVS Pharmacy, Inc.

One CVS Drive, Woonsocket, RI 02895

CVS.com® 1-800-SHOP CVS

Made in the U.S.A. of U.S. and imported components

V-31490

CVS® Quality

Money Back Guarantee

#975032

M050779CP

Principal Display Panel - Carton Label

SKIN+PHARMACY

ADVANCED

ACNE THERAPY KIT

$35 VALUE

$19.99

BONUS:

Includes 2 Gentle Facial

Cleansing Sponges

exclusively at

CVS/pharmacy

ONE MONTH SUPPLY

Actual Size Product Shown

Principal Display Panel - Clarifying Daily Cleanser Tube Label

SKIN+PHARMACY

ADVANCED

ACNE

THERAPY

CLARIFYING

DAILY CLEANSER

with Polytrap® Technology

Maximum Strength

2% Salicylic Acid

removes excess skin oils
unclogs pores
oil-free formula

DERMATOLOGIST TESTED

exclusively at

CVS/pharmacy

4 FL OZ (118 mL)

Principal Display Panel - Clarifying Daily Cleanser Tube Label

Principal Display Panel - Active Clearing Lotion Tube Label

SKIN+PHARMACY

ADVANCED

ACNE

THERAPY

ACTIVE CLEARING LOTION

with Microsponge® Technology

clinically proven to kill acne-causing bacteria
clinically proven to effectively reduce inflammatory lesions
soothing, oil-free formula
unclogs pores
fragrance free

DERMATOLOGIST TESTED

exclusively at

CVS/pharmacy

0.75 FL OZ (22 mL)

Principal Display Panel - Active Clearing Lotion Tube Label

Principal Display Panel - Spot Treatment Tube Label

SKIN+PHARMACY

ADVANCED

ACNE

THERAPY

SPOT TREATMENT

with Microsponge® Technology

5% Benzoyl Peroxide

clinically proven to effectively reduce inflammatory lesions
effectively kills acne-causing bacteria
helps reduce irritation
fragrance free

DERMATOLOGIST TESTED

exclusively at

CVS/pharmacy

0.4 FL OZ (12 mL)

Principal Display Panel - Spot Treatment Tube Label

INGREDIENTS AND APPEARANCE

SKINPHARMACY ADVANCED ACNE THERAPY KIT

salicylic acid, benzoyl peroxide kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69842-082

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69842-082-01	1 in 1 CARTON; Type 0: Not a Combination Product	10/01/2014

Part #	Package Quantity	Total Product Quantity
Quantity of Parts
Part 1	1 TUBE	118 mL
Part 2	1 TUBE	22 mL
Part 3	1 TUBE	12 mL

Part 1 of 3
SKINPHARMACY ADVANCED ACNE THERAPY CLARIFYING DAILY CLEANSER salicylic acid liquid

Product Information
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
Water (UNII: 059QF0KO0R)
sodium C14-16 olefin sulfonate (UNII: O9W3D3YF5U)
polyethylene glycol 4000 (UNII: 4R4HFI6D95)
cocamidopropyl betaine (UNII: 5OCF3O11KX)
Xanthan gum (UNII: TTV12P4NEE)
DMDM Hydantoin (UNII: BYR0546TOW)
edetate disodium (UNII: 7FLD91C86K)
.alpha.-tocopherol acetate, DL- (UNII: WR1WPI7EW8)
Hamamelis virginiana flower water (UNII: 222MYC9QUV)
Butylene glycol (UNII: 3XUS85K0RA)
Calendula Officinalis flower (UNII: P0M7O4Y7YD)
licorice (UNII: 61ZBX54883)
Phenoxyethanol (UNII: HIE492ZZ3T)
FD&C Yellow No. 5 (UNII: I753WB2F1M)
FD&C red no. 40 (UNII: WZB9127XOA)
Lauryl Methacrylate/Glycol Dimethacrylate Crosspolymer (UNII: EX0F4CZ66H)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1		118 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	10/01/2014

Part 2 of 3
SKINPHARMACY ADVANCED ACNE THERAPY ACTIVE CLEARING benzoyl peroxide lotion

Product Information
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
benzoyl peroxide (UNII: W9WZN9A0GM) (benzoyl peroxide - UNII:W9WZN9A0GM)	benzoyl peroxide	25 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
water (UNII: 059QF0KO0R)
glycerin (UNII: PDC6A3C0OX)
methyl methacrylate/glycol dimethacrylate crosspolymer (UNII: EG97988M5Q)
cetyl alcohol (UNII: 936JST6JCN)
sorbitol (UNII: 506T60A25R)
glyceryl dilaurate (UNII: MFL3ZIE8SK)
stearyl alcohol (UNII: 2KR89I4H1Y)
magnesium aluminum silicate (UNII: 6M3P64V0NC)
sodium citrate (UNII: 1Q73Q2JULR)
silicon dioxide (UNII: ETJ7Z6XBU4)
sodium lauryl sulfate (UNII: 368GB5141J)
citric acid monohydrate (UNII: 2968PHW8QP)
methylparaben (UNII: A2I8C7HI9T)
xanthan gum (UNII: TTV12P4NEE)
propylparaben (UNII: Z8IX2SC1OH)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1		22 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	10/01/2014

Part 3 of 3
SKINPHARMACY ADVANCED ACNE THERAPY SPOT TREATMENT benzoyl peroxide lotion

Product Information
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
benzoyl peroxide (UNII: W9WZN9A0GM) (benzoyl peroxide - UNII:W9WZN9A0GM)	benzoyl peroxide	50 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
water (UNII: 059QF0KO0R)
glycerin (UNII: PDC6A3C0OX)
methyl methacrylate/glycol dimethacrylate crosspolymer (UNII: EG97988M5Q)
cetyl alcohol (UNII: 936JST6JCN)
sorbitol (UNII: 506T60A25R)
glyceryl dilaurate (UNII: MFL3ZIE8SK)
stearyl alcohol (UNII: 2KR89I4H1Y)
magnesium aluminum silicate (UNII: 6M3P64V0NC)
sodium citrate (UNII: 1Q73Q2JULR)
silicon dioxide (UNII: ETJ7Z6XBU4)
sodium lauryl sulfate (UNII: 368GB5141J)
citric acid monohydrate (UNII: 2968PHW8QP)
methylparaben (UNII: A2I8C7HI9T)
xanthan gum (UNII: TTV12P4NEE)
propylparaben (UNII: Z8IX2SC1OH)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1		12 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	10/01/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	10/01/2014

Labeler - CVS Health (062312574)

Registrant - AMCOL Health & Beauty Solutions, Inc. DBA (872684803)

Name	Address	ID/FEI	Business Operations
Establishment
AMCOL Health & Beauty Solutions, Inc. DBA		872684803	ANALYSIS(69842-082) , MANUFACTURE(69842-082) , LABEL(69842-082) , PACK(69842-082)

Revised: 3/2017

Document Id: 80cecb53-6a09-4802-95fd-8d4130be8aa7

Set id: a8c8cde4-c2bf-42aa-a3d1-a1846732e5e2

Version: 1

Effective Time: 20170314

Search by Drug Name or NDC

NDC 69842-0082-01 SkinPharmacy Advanced Acne Therapy Kit Details

SkinPharmacy Advanced Acne Therapy Kit

MedlinePlus Drug Summary

Product Information

Package

Package Images

NDC 69842-0082-01 (69842008201)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL a8c8cde4-c2bf-42aa-a3d1-a1846732e5e2 Details

SPL UNCLASSIFIED SECTION

Active Ingredient

Purpose

Use

Warnings

Ask a doctor or pharmacist before use if you are

When using this product

Directions

Inactive ingredients

SPL UNCLASSIFIED SECTION

Active Ingredient

Purpose

Use

Warnings

Do not use this medication if you

When using this product

Directions

Inactive ingredients

SPL UNCLASSIFIED SECTION

Active Ingredient

Purpose

Use

Warnings

Do not use this medication if you

When using this product

Directions

Inactive ingredients

Principal Display Panel - Carton Label

Principal Display Panel - Clarifying Daily Cleanser Tube Label

Principal Display Panel - Active Clearing Lotion Tube Label

Principal Display Panel - Spot Treatment Tube Label

INGREDIENTS AND APPEARANCE