TARGET UP AND UP 3 STEP ACNE SYSTEM- benzoyl peroxide 
TARGET CORPORATION

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.

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Target Up and Up 3 Step Acne System

Active ingredient

Benzoyl Peroxide 2.5%

Purpose

Acne Treatment

Uses

for the management of acne

​Warnings

For external use only.

Do not use if you

  • have very sensitive skin
  • 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. • 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.

​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

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

Benzoyl Peroxide 2.5%

Purpose

Acne Treatment

Uses

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

• 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.

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

•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.

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

82087K3

82091E5

82093E4

TARGET UP AND UP 3 STEP ACNE SYSTEM 
benzoyl peroxide kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-152
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-152-981 in 1 KIT07/07/2016
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE 118.2 mL
Part 21 BOTTLE 59.1 mL
Part 1 of 2
STEP 1 RENEWING CLEANSER 
benzoyl peroxide lotion
Product Information
Item Code (Source)NDC:11673-162
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE2.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
STEARETH-2 (UNII: V56DFE46J5)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C)  
WATER (UNII: 059QF0KO0R)  
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
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)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
PETROLATUM (UNII: 4T6H12BN9U)  
LAURETH-4 (UNII: 6HQ855798J)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-162-53118.2 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM00607/07/2016
Part 2 of 2
STEP 3 REPAIRING TREATMENT 
benzoyl peroxide lotion
Product Information
Item Code (Source)NDC:11673-161
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE2.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-161-6159.1 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM00607/07/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM00607/07/2016
Labeler - TARGET CORPORATION (006961700)

Revised: 3/2023
Document Id: f784bda2-1181-574c-e053-6394a90a6d9f
Set id: f784bd99-0b8a-2521-e053-6294a90a2519
Version: 1
Effective Time: 20230322
 
TARGET CORPORATION