3 Step Acne System Well At Walgreens: Package Insert and Label Information

3 STEP ACNE SYSTEM WELL AT WALGREENS- benzoyl peroxide
Walgreens

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active ingredient Purpose

Benzoyl Peroxide — 2.50% Acne Treatment

Uses

• Treats and helps prevent acne blemishes.

​Warnings For external use only.

Do not use if you have very sensitive skin or if you are sensitive to benzoyl peroxide.

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. • rinse right away with water if it gets in eyes • avoid unnecessary sun exposure and use a sunscreen •avoid contact with eyes, lips, and mouth • avoid contact with hair and dyed fabrics, which may be bleached by this product • skin irritation may occurs, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

​Stop use and ask a doctor if ​ irritation becomes severe.

Keep out of reach of the children

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

Directions

Use morning and night. Apply a small (dime-sized) amount to dampened skin and gently massage. Rinse thoroughly with warm water. If bothersome dryness or peeling occurs, reduce application use. Follow with Refreshing Toner.

Inactive ingredients

Water, Magnesium Aluminum Silicate, Glyceryl Stearate, PEG-100 Stearate, Sorbitol, Dimethyl Isosorbide, Disodium PEG-12 Dimethicone Sulfosuccinate, Tridecyl Stearate, Neopentyl Glycol Dicaprylate/Dicaprate, Polyethylene, Cetyl Esters, Anthemis Nobilis Flower Extract,
Sodium Hyaluronate, Sodium PCA, Xanthan Gum, Tridecyl Trimellitate, Propylene Glycol, Imidazolidinyl Urea, Methylparaben, Propylparaben,
Fragrance

Active ingredient Purpose

Benzoyl Peroxide — 2.50% Acne Treatment

Uses

• Treats and helps prevent acne blemishes.

Warnings For external use only.

Do not use if you have very sensitive skin or if you are sensitive to benzoyl peroxide.

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. • rinse right away with water if it gets in eyes • avoid unnecessary sun exposure and use a sunscreen •avoid contact with eyes, lips, and mouth • avoid contact with hair and dyed fabrics, which may be bleached by this product • skin irritation may occurs, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

Stop use and ask a doctor if irritation becomes severe.

Keep out of reach of the children

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

Directions

• Cleans the skin thoroughly before applying medication • Cover the entire affected area one to three times a day • 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. • If going outside, use a sunscreen. If sensitivity develops, discontinue use of both products and consult a doctor.

Inactive ingredients

Water, Ethoxydiglycol, Cyclotetrasiloxane, Cyclopentasiloxane, Cetearyl Alcohol, Propylene Glycol, Dimethicone, lyceryl Stearate, PEG-100 Stearate, Panthenol, Allantoin, Xanthan Gum, Ceteareth-20, Carbomer, Triethanolamine, Diazolidinyl Urea, Methylparaben, Propylparaben,
Fragrance

image description
(click image for full-size original)

Ucarton back
(click image for full-size original)
3 STEP ACNE SYSTEM WELL AT WALGREENS
benzoyl peroxide kit
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-3226
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0363-3226-07 1 KIT in 1 KIT None
Quantity of Parts
Part # Package Quantity Total Product Quantity
Part 1 1 BOTTLE 120 mL
Part 2 1 BOTTLE 60 mL
Part 1 of 2
CLARIFYING CLEANSER STEP 1
benzoyl peroxide lotion
Product Information
Item Code (Source) NDC:0363-3227
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Benzoyl Peroxide (BENZOYL PEROXIDE) Benzoyl Peroxide 2.5 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
Water
Magnesium Aluminum Silicate
GLYCERYL MONOSTEARATE
PEG-100 Stearate
Sorbitol
Dimethyl Isosorbide
Tridecyl Stearate
Neopentyl Glycol Dicaprylate/Dicaprate
HIGH DENSITY POLYETHYLENE
CETYL ESTERS WAX
CHAMAEMELUM NOBILE FLOWER
HYALURONATE SODIUM
SODIUM PYRROLIDONE CARBOXYLATE
Xanthan Gum
Tridecyl Trimellitate
Propylene Glycol
IMIDUREA
Methylparaben
Propylparaben
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0363-3227-04 120 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333D 07/15/2014
Part 2 of 2
REPAIRTHERAPY STEP 3
benzoyl peroxide lotion
Product Information
Item Code (Source) NDC:0363-3228
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Benzoyl Peroxide (BENZOYL PEROXIDE) Benzoyl Peroxide 2.5 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
Water
DIETHYLENE GLYCOL MONOETHYL ETHER
CYCLOMETHICONE 4
CYCLOMETHICONE 5
CETOSTEARYL ALCOHOL
Propylene Glycol
Dimethicone
GLYCERYL MONOSTEARATE
PEG-100 Stearate
Panthenol
Allantoin
Xanthan Gum
POLYOXYL 20 CETOSTEARYL ETHER
TROLAMINE
Diazolidinyl Urea
Methylparaben
Propylparaben
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0363-3228-02 60 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333D 07/15/2014
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333D 07/15/2014
Labeler — Walgreens (008965063)
Registrant — Product Quest Mfg (927768135)
Establishment
Name Address ID/FEI Operations
Product Quest Mfg 927768135 manufacture (0363-3226), label (0363-3226), pack (0363-3226)

Revised: 02/2018 Walgreens

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.