TARGET UP AND UP DAILY MOISTURIZING- dimethicone lotion

Target Up and Up Daily Moisturizing by

Drug Labeling and Warnings

Target Up and Up Daily Moisturizing by is a Otc medication manufactured, distributed, or labeled by TARGET CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Dimethicone 1.2%

Purpose

Skin Protectant

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures (see  Directions), decreases the risk of skin cancer and early skin aging caused by the sun

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

• apply as needed to hands or body when skin feels dry or irritated

Other information

• may stain some fabrics

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

INGREDIENTS AND APPEARANCE

TARGET UP AND UP DAILY MOISTURIZING 
dimethicone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-087
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	12 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-087-18	85 mL in 1 TUBE; Type 0: Not a Combination Product	05/01/2009
2	NDC: 11673-087-98	2 in 1 PACKAGE	05/01/2009
2	NDC: 11673-087-43	532 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	M016	05/01/2009

Labeler - TARGET CORPORATION (006961700)