CITY SUNSCREEN SERUM BROAD SPECTRUM SPF 30 SUPERGOOP- homos alate, octisalate, avobenzene, octocrylene cream Baxter Laboratories Pty. Ltd.

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CITY SUNSCREEN SERUM BROAD SPECTRUM SPF 30 SUPERGOOP- homos alate, octisalate, avobenzene, octocrylene cream Baxter Laboratories Pty. Ltd. 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. ---------- City Suns creen Serum Broad Spectrum SPF 30 Active ingredients: Purpose Homosalate 8%, Octisalate 4%, Avobenzene 3%, Octocrylene 2% Sunscreen Purpose Uses Simultaneously protects skin, combats premature aging and moisturizes on contact helps prevent sunburn If used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging skin aging caused by the sun Keep out of reach of children Warnings For external use only. Do not use on damaged or broken skin When using this product, keep out of of eyes. Rinse with water to remove. If swallowed, get medical help or contact a Poison Control Center right away. Directions: Apply liberally 15 minutes before sun exposure Use a water resistant sunscreen if swimming or sweating Reapply 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 sunscreenwith Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun,especially from 10 a.m. -2p.m. Wear long-sleeved shirts, pants, hats, and sunglasses Inactive Ingredients Purified water (Aqua), Cyclometicone, Isostearyl Neopentanoate, Glycerin, Ceteareth-20, Polypropylene, Cetearyl Alcohol, Xanthan Gum, d-panthenol, Octanohydroxamic acid, Caprylyl Glycol, Silica, Triacontanyl PVP, Cetyl Dimethicone, Ammonium Acryloyldimethyltaurate/VP Copolymer, PEG-40 Stearate, Tocopheryl, Disodium EDTA, Pentylene Glycol, Pantheyl Triacetate, Sodium Lactate, Lactic Acid, Serine, Urea, Sorbitol, Sodium Chloride, Allantoin, Oleyl Alcohol, Ethyl Linoleate. City Sunscreen SERUM With Vitamins E & B5 Supergoop!

CITY SUNSCREEN SERUM BROAD SPECTRUM SPF 30 SUPERGOOP homosalate, octisalate, avobenzene, octocrylene cream Product Information Product T ype HUMAN OTC DRUG Ite m Code (Source ) NDC:70 157-0 0 2 Route of Ad minis tration TOPICAL Active Ing redient/active Moiety Ing redient Name Basis o f Streng th Streng th HO MO SALATE (UNII: V0 6 SV4M9 5S) (HOMOSALATE - UNII:V0 6 SV4M9 5S) HOMOSALATE 8 g in 10 0 ml O CTISALATE (UNII: 4X49 Y0 59 6 W) (OCTISALATE - UNII:4X49 Y0 59 6 W) OCTISALATE 4 g in 10 0 ml AVO BENZO NE (UNII: G6 3QQF2NOX) (AVOBENZONE - UNII:G6 3QQF2NOX) AVOBENZONE 3 g in 10 0 ml O CTO CRYLENE (UNII: 5A6 8 WGF6 WM) (OCTOCRYLENE - UNII:5A6 8 WGF6 WM) OCTOCRYLENE 2 g in 10 0 ml Inactive Ing redients Ing redient Name CYCLO METHICO NE (UNII: NMQ3479 9 4Z) GLYCERIN (UNII: PDC6 A3C0 OX) XANTHAN GUM (UNII: TTV12P4NEE) PANTHENO L (UNII: WV9 CM0 O6 7Z) CAPRYLYL GLYCO L (UNII: 0 0 YIU5438 U) Streng th

SILICO N DIO XIDE (UNII: ETJ7Z6 XBU4) PO LYO XYL 4 0 STEARATE (UNII: 13A4J4NH9 I) EDETATE DISO DIUM (UNII: 7FLD9 1C8 6 K) PENTYLENE GLYCO L (UNII: 50 C130 7PZG) SO DIUM LACTATE (UNII: TU7HW0 W0 QT) LACTIC ACID (UNII: 33X0 4XA5AT) SERINE (UNII: 452VLY9 40 2) UREA (UNII: 8 W8 T178 47W) SO RBITO L (UNII: 50 6 T6 0 A25R) SO DIUM CHLO RIDE (UNII: 451W47IQ8 X) ALLANTO IN (UNII: 344S277G0 Z) O LEYL ALCO HO L (UNII: 172F2WN8 DV) ETHYL LINO LEATE (UNII: MJ2YTT4J8 M) Packag ing # Item Co de Packag e Descriptio n 1 2 3 4 5 6 0 1 0 2 0 3 0 4 0 5 0 6 50 ml in 1 BOTTLE, PUMP; Type 0 : No t a Co mbinatio n Pro duct 20 ml in 1 BOTTLE, PUMP; Type 0 : No t a Co mbinatio n Pro duct Marketing Start Date 12/0 7/20 10 12/0 7/20 10 10 ml in 1 TUBE; Type 0 : No t a Co mbinatio n Pro duct 12/0 7/20 10 6 0 ml in 1 TUBE; Type 0 : No t a Co mbinatio n Pro duct 12/0 7/20 10 3 ml in 1 PACKET; Type 0 : No t a Co mbinatio n Pro duct 12/0 7/20 10 15 ml in 1 TUBE; Type 0 : No t a Co mbinatio n Pro duct 0 7/19 /20 16 Marketing End Date Marketing Information Marke ting Cate gory Application Numbe r or Monograph Citation Marke ting Start Date Marke ting End Date OTC mo no graph final part352 12/0 7/20 10 Labeler - Baxter Laboratories Pty. Ltd. (740537709) Registrant - Baxter Laboratories Pty. Ltd. (740537709) Establishment Name Addre ss ID/FEI Busine ss Ope rations Baxter Labo rato ries Pty. Ltd. 740 53770 9 manufacture(70 157-0 0 2) Revised: 1/2017 Baxter Laboratories Pty. Ltd.