UP AND UP DUAL EFFECTS MOISTURIZER- salicylic acid lotion 
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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Up & Up Dual Effects Moisturizer

Active ingredient

Salicylic Acid 0.5%

Purpose

Acne Medication

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

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 doctor. • If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Other information

• may stain some fabrics

Inactive ingredients

Water, Dicaprylyl Ether, Glycerin, Cetearyl Alcohol, Dimethicone, Neopentyl Glycol Diisostearate, Neopentyl Glycol Diethylhexanoate, Aluminum Starch Octenylsuccinate, Methyl Gluceth-20, Dicetyl Phosphate, Ceteth-10 Phosphate, Mentyl Lacatate, Steareth-21, Steareth-2, Fragrance, Xanthan Gum, Disodium EDTA, Sodium Hydroxide, Magnesium Aluminum Silicate, BHT.

82582E5

82582F5

UP AND UP  DUAL EFFECTS MOISTURIZER
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-931
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
STEARETH-2 (UNII: V56DFE46J5)  
GLYCERIN (UNII: PDC6A3C0OX)  
DICAPRYLYL ETHER (UNII: 77JZM5516Z)  
WATER (UNII: 059QF0KO0R)  
STEARETH-21 (UNII: 53J3F32P58)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW)  
CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)  
NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)  
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
XANTHAN GUM (UNII: TTV12P4NEE)  
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-931-53118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/11/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D10/11/2012
Labeler - TARGET CORPORATION (006961700)

Revised: 10/2022
Document Id: ea2b2e08-0d80-6027-e053-2995a90a806c
Set id: 933feba6-df4b-ebb9-e053-2995a90af459
Version: 3
Effective Time: 20221003
 
TARGET CORPORATION