Label: SOFT FOCUS CITY SUNCREEN SERUM BROAD SPECTRUM SPF 30 SUPERGOOP- avobenzone, homosalate, octisalate, octocrylene liquid
- NDC Code(s): 70157-005-01, 70157-005-02
- Packager: Baxter Laboratories Pty. Ltd.
- 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 November 22, 2022
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- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions
Apply two pumps to face and neckat least 15 minutes prior to sun exposure. Oil-free and fast absorbing, it's ideal for use alone or as a smoothing primer under the rest of your skincare regimen. Use a water resistant sunscreen if swimming or sweating
Reapply at least every 2 hours
Children under 6 months: Ask a doctor
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INACTIVE INGREDIENT
Inactive Ingredients Aqua, Cyclopentasilosiloxane, Isostearyl Neopentanoate, Glycerin, Cyclohexasiloxane, Ceteareth-20, Polypropylene, Cetearyl Alcohol, Caprylyl Glycol, Xanthan Gum, PEG-40 Stearate, Triacontanyl PVP, Silica, Ammonium Acryloyldimethyltaurate/VP Copolymer, Panthenyl Triacetate, Cetyl Dimethicone, Ethyl Linoleate, Caprylhydroxamic Acid, Oleyl Alcohol, Tocopherol, Disodium EDTA, Panthenol, Triethanolamine, Pentylene Glycol, Sodium Lactate, Lactic Acid, Serine, Urea, Sorbitol, Sodium Chloride, Allantoin, CI 77492, CI77491, CI77499
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SOFT FOCUS CITY SUNCREEN SERUM BROAD SPECTRUM SPF 30 SUPERGOOP
avobenzone, homosalate, octisalate, octocrylene liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70157-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 8 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 2 g in 100 mL Inactive Ingredients Ingredient Name Strength AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) PANTHENOL TRIACETATE, (+)- (UNII: 1206E8961B) CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) ETHYL LINOLEATE (UNII: MJ2YTT4J8M) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) OLEYL ALCOHOL (UNII: 172F2WN8DV) TOCOPHEROL (UNII: R0ZB2556P8) EDETATE DISODIUM (UNII: 7FLD91C86K) PANTHENOL (UNII: WV9CM0O67Z) TROLAMINE (UNII: 9O3K93S3TK) PENTYLENE GLYCOL (UNII: 50C1307PZG) SODIUM LACTATE (UNII: TU7HW0W0QT) LACTIC ACID (UNII: 33X04XA5AT) SERINE (UNII: 452VLY9402) UREA (UNII: 8W8T17847W) SORBITOL (UNII: 506T60A25R) SODIUM CHLORIDE (UNII: 451W47IQ8X) ALLANTOIN (UNII: 344S277G0Z) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ISOSTEARYL NEOPENTANOATE (UNII: 411THY156Q) CYCLOMETHICONE 6 (UNII: XHK3U310BA) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CAPRYLYL GLYCOL (UNII: 00YIU5438U) XANTHAN GUM (UNII: TTV12P4NEE) PEG-40 STEARATE (UNII: ECU18C66Q7) TRICONTANYL POVIDONE (UNII: N0SS3Q238D) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70157-005-02 1 in 1 CARTON 12/30/2014 1 NDC:70157-005-01 60 mL 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 12/30/2014 Labeler - Baxter Laboratories Pty. Ltd. (740537709) Registrant - Baxter Laboratories Pty. Ltd. (740537709)