Label: TARGET UP AND UP 3 STEP ACNE SYSTEM- benzoyl peroxide kit
- NDC Code(s): 11673-152-98, 11673-161-61, 11673-162-53
- Packager: TARGET CORPORATION
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 14, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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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 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 occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.
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Directions
- Sensitivity Test for a New User: Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated below.
- cover the entire affected area with a thin layer, massaging gently one to two minutes, and rinse thoroughly one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to 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, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.
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Inactive ingredients
WATER, PETROLATUM, CETYL ALCOHOL, HYDROGENATED SOYBEAN OIL, PROPYLENE GLYCOL, BENZYL ALCOHOL, LAURETH-4, POTASSIUM CETYL PHOSPHATE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, MAGNESIUM ALUMINUM SILICATE, GLYCERYL STEARATE, PEG-100 STEARATE, CETYL ESTERS, STEARETH-2, SORBITOL, SODIUM PCA, ANTHEMIS NOBILIS FLOWER EXTRACT, SODIUM HYALURONATE, DISODIUM EDTA, XANTHAN GUM, TRIDECYL STEARATE, NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE, TRIDECYL TRIMELLITATE, DIMETHYL ISOSORBIDE, FRAGRANCE.
- Active ingredient
- Purpose
- Uses
-
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 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.
-
Directions
•Sensitivity Test for a New User: Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated below.
- cleanthe 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 to 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, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.
-
Inactive ingredients
WATER, CETEARYL ALCOHOL, PETROLATUM, BENZYL ALCOHOL, POTASSIUM CETYL PHOSPHATE, STEARETH-2, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, PANTHENOL, ALLANTOIN, PROPYLENE GLYCOL, XANTHAN GUM, DIMETHICONE, GLYCERYL STEARATE, PEG-100 STEARATE, CYCLOTETRASILOXANE, CYCLOPENTASILOXANE, ETHOXYDIGLYCOL, FRAGRANCE.
- Label
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INGREDIENTS AND APPEARANCE
TARGET UP AND UP 3 STEP ACNE SYSTEM
benzoyl peroxide kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-152 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-152-98 1 in 1 KIT 07/07/2016 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 118.2 mL Part 2 1 BOTTLE 59.1 mL Part 1 of 2 STEP 1 RENEWING CLEANSER
benzoyl peroxide lotionProduct Information Item Code (Source) NDC:11673-162 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 2.5 g in 100 mL Inactive Ingredients Ingredient Name Strength STEARETH-2 (UNII: V56DFE46J5) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C) WATER (UNII: 059QF0KO0R) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) PEG-100 STEARATE (UNII: YD01N1999R) SORBITOL (UNII: 506T60A25R) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) TRIDECYL STEARATE (UNII: A8OE252M6L) NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K) CETYL ESTERS WAX (UNII: D072FFP9GU) CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) XANTHAN GUM (UNII: TTV12P4NEE) TRIDECYL TRIMELLITATE (UNII: FY36J270ES) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) EDETATE DISODIUM (UNII: 7FLD91C86K) CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36) CETYL ALCOHOL (UNII: 936JST6JCN) PETROLATUM (UNII: 4T6H12BN9U) LAURETH-4 (UNII: 6HQ855798J) BENZYL ALCOHOL (UNII: LKG8494WBH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-162-53 118.2 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 07/07/2016 Part 2 of 2 STEP 3 REPAIRING TREATMENT
benzoyl peroxide lotionProduct Information Item Code (Source) NDC:11673-161 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 2.5 g in 100 mL Inactive Ingredients Ingredient Name Strength CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36) BENZYL ALCOHOL (UNII: LKG8494WBH) PETROLATUM (UNII: 4T6H12BN9U) STEARETH-2 (UNII: V56DFE46J5) WATER (UNII: 059QF0KO0R) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) CYCLOMETHICONE 4 (UNII: CZ227117JE) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) PANTHENOL (UNII: WV9CM0O67Z) ALLANTOIN (UNII: 344S277G0Z) XANTHAN GUM (UNII: TTV12P4NEE) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-161-61 59.1 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 07/07/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 07/07/2016 Labeler - TARGET CORPORATION (006961700)
