Label: TARGET UP AND UP SPF50 SPORT SUNSCREEN LIP BALM REEF-CONSCIOUS FORMULA- avobenzone, homosalate, octocrylene stick
- NDC Code(s): 11673-168-56, 11673-168-58, 11673-168-84, 11673-168-91
- Packager: TARGET CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated April 7, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
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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
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Inactive ingredients
Petrolatum, Polyethylene, Ethylhexyl Palmitate, Trimethylsiloxyphenyl Dimethicone, Microcrystalline Wax, Butyloctyl Salicylate, Isopropyl Myristate, Theobroma Cacao (Cocoa) Seed Butter, Mineral Oil, PEG-8, Caprylyl Glycol, Cocos Nucifera (Coconut) Oil, Sodium Saccharin, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate.
- Labels
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INGREDIENTS AND APPEARANCE
TARGET UP AND UP SPF50 SPORT SUNSCREEN LIP BALM REEF-CONSCIOUS FORMULA
avobenzone, homosalate, octocrylene stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-168 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 80 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 g Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) PETROLATUM (UNII: 4T6H12BN9U) SACCHARIN SODIUM ANHYDROUS (UNII: I4807BK602) COCONUT OIL (UNII: Q9L0O73W7L) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ETHYLHEXYL PALMITATE (UNII: 2865993309) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) COCOA BUTTER (UNII: 512OYT1CRR) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ALOE VERA LEAF (UNII: ZY81Z83H0X) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-168-84 4 in 1 PACKAGE 12/21/2018 1 NDC:11673-168-56 17 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:11673-168-91 2 in 1 PACKAGE 12/21/2018 2 NDC:11673-168-58 4.25 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M020 12/21/2018 Labeler - TARGET CORPORATION (006961700)