TARGET UP AND UP DAILY MOISTURIZING- dimethicone 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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Target Up & Up Daily Moisturizing Lotion

Active ingredients

Dimethicone 1.2%

Purpose

Skin Protectant

Uses

Warnings

For external use only

Do not use

• deep or puncture wounds • animal bites • serious burns

When using this product

• keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

• condition worsens • symptoms last more than seven days or clear up and occur again within a few days

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

avena sativa (oat) kernel flour, behenrimonium chloride, benzyl alcohol, cetearyl alcohol, cetyl alcohol, glycerin, isopropyl palmitate, petrolatum, polyquaterium-37, sodium chloride, water.

Label

82845E8F9

TARGET UP AND UP DAILY MOISTURIZING 
dimethicone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-087
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE12 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
POLYQUATERNIUM 37 (200 MPA.S) (UNII: 67C1D6YV24)  
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
PETROLATUM (UNII: 4T6H12BN9U)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
OATMEAL (UNII: 8PI54V663Y)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-087-1885 mL in 1 TUBE; Type 0: Not a Combination Product05/01/2009
2NDC:11673-087-982 in 1 PACKAGE05/01/2009
2NDC:11673-087-43532 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM01605/01/2009
Labeler - TARGET CORPORATION (006961700)

Revised: 4/2023
Document Id: f907010c-6789-e51b-e053-6394a90a8f8a
Set id: f118e0eb-1e66-50ab-e053-2995a90a2cb9
Version: 3
Effective Time: 20230410
 
TARGET CORPORATION