Label: TARGET UP AND UP KIDS MINERAL SUNSCREEN SPF 50- titanium dioxide, zinc oxide lotion
- NDC Code(s): 11673-089-40
- Packager: TARGET CORPORATION
- Category: HUMAN OTC DRUG LABEL
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 February 9, 2021
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask 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: 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 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 sleeve shirts, pants, hats, and sunglasses
- Other infomation
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Inactive Ingredients
water, caprylic/capric triglyceride, isohexadecane, butyloctyl salicylate, octyldodecyl citrate crosspolymer, cetyl PEG/PPG-10/1 dimethicone, lauryl PEG-8 dimethicone, C30-38 olefin/isopropyl maleate/MA copolymer, sodium chloride, ethylhexyl methoxycrylene, dimethicone, caprylyl glycol, PEG-8, silica, triethoxycaprylylsilane, glycerin, sodium citrate, tocopheryl acetate, benzyl alcohol, benzoic acid, sorbic acid.
- Label
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INGREDIENTS AND APPEARANCE
TARGET UP AND UP KIDS MINERAL SUNSCREEN SPF 50
titanium dioxide, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-089 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 65 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 45 mg in 1 mL Inactive Ingredients Ingredient Name Strength OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: X323T6QO4M) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) SORBIC ACID (UNII: X045WJ989B) WATER (UNII: 059QF0KO0R) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT) SODIUM CHLORIDE (UNII: 451W47IQ8X) GLYCERIN (UNII: PDC6A3C0OX) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) BENZYL ALCOHOL (UNII: LKG8494WBH) 1,5-PENTANEDIOL (UNII: 07UXZ0SCST) SODIUM CITRATE (UNII: 1Q73Q2JULR) BENZOIC ACID (UNII: 8SKN0B0MIM) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ISOHEXADECANE (UNII: 918X1OUF1E) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) DIMETHICONE (UNII: 92RU3N3Y1O) LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX) POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-089-40 308 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/17/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/17/2014 Labeler - TARGET CORPORATION (006961700)