TARGET UP AND UP BROAD SPECTRUM SPF 55 OIL-FREE- avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion

Target Up and Up Broad Spectrum SPF 55 Oil-Free by

Drug Labeling and Warnings

Target Up and Up Broad Spectrum SPF 55 Oil-Free by is a Otc medication manufactured, distributed, or labeled by TARGET CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Avobenzone 2.7%

Homosalate 4.0%

Octisalate 4.5%

Octocrylene 6.0%

Oxybenzone 4.5%

Purpose

Sunscreen

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

• on damaged or broken skin

​When using this product​

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

Stop use and ask doctor if​

• ​rash occurs.

​Keep out of reach of children.

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

Directions

• apply liberally 15 minutes before sun exposure

• reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours

• children under 6 months of age: Ask a doctor

• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
• limit time in the sun, especially from 10 a.m. - 2 p.m.
• wear long-sleeved shirts, pants, hats, and sunglasses

Other information

protect the product in this container from excessive heat and direct sun
may stain or damage some fabrics, materials or surfaces

Inactive ingredients

acrylates/dimethicone copolymer, BHT, bisabolol, butylene glycol, C12-15 alkyl benzoate, capryloyl glycine, caprylyl glycol, cedrus atlantica bark extract, cetyl
dimethicone, chlorphenesin, cinnamomum zeylanicum bark extract, dimethicone,
disodium EDTA, ethylhexyl stearate, ethylhexylglycerin, glycerin, mannan,
neopentyl glycol diheptanoate, phenoxyethanol, polyester-7, portulaca oleracea
extract, propylene glycol, sarcosine, silica, sodium polyacrylate, steareth-100,
steareth-2, styrene/acrylates copolymer, trideceth-6, water, xanthan gum

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TARGET UP AND UP BROAD SPECTRUM SPF 55 OIL-FREE 
avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-146
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	27 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	40 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	45 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	60 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	45 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE (UNII: 92RU3N3Y1O)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
KONJAC MANNAN (UNII: 36W3E5TAMG)
PURSLANE (UNII: M6S840WXG5)
CHLORPHENESIN (UNII: I670DAL4SZ)
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CETYL DIMETHICONE 45 (UNII: IK315POC44)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
STEARETH-2 (UNII: V56DFE46J5)
WATER (UNII: 059QF0KO0R)
STEARETH-100 (UNII: 4OH5W9UM87)
XANTHAN GUM (UNII: TTV12P4NEE)
POLYESTER-7 (UNII: 0841698D2F)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF)
SARCOSINE (UNII: Z711V88R5F)
CINNAMON BARK OIL (UNII: XE54U569EC)
FARNESOL (UNII: EB41QIU6JL)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-146-09	88 mL in 1 TUBE; Type 0: Not a Combination Product	01/29/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	01/29/2014

Labeler - TARGET CORPORATION (006961700)