- active information
- Purpose
- Use
- Warnings
- Do not use
- When using this product
- stop use and ask a doctor if
- Keep out of reach of children
-
Directions
- apply liberally 15 minures before sun exposure
- reapply at least every 2 hours:
- use a water resistant sunscreen if swimming or sweating
- Sun Protection Measures. Spending time in the sun increases your risk of cancer and early skin aging. To decrease this risk, regularly use a sunscreen with Broad Spectrum SPF Value of 15 or higher and other sun protection measures including:
- limit the time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeved shirts, pants hats and sunglasses
- children umder 6 months of age: ask a doctor
- Other information
-
Inactive ingredients
water, C12-15 alkyl benzoate, cetearyl alcohol, glycerin, dimethicone, Glycine soja (soybean) seed extract, bis-phenylpropyl dimethicone, arachidyl alcohol, cetearyl glucoside, benzyl alcohol, panthenol, ethylene/acrylic acid copolymer, behenyl alcohol, steareth-2, fragrance, steareth-21, polymethyl methacrylate, polyacrylamide, arachidyl glucoside, disodium EDTA, C13-14 isoparaffin, laureth-7, silica, chlorphenesin, BHT, titanium dioxide, mica
- Adverse Reactions Section
- principal display panel
-
INGREDIENTS AND APPEARANCE
DAILY MOISTURIZER
octinoxate, octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72288-338 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) SOYBEAN (UNII: L7HT8F1ZOD) BIS-PHENYLPROPYL DIMETHICONE (15 CST) (UNII: 4836494CFT) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) BENZYL ALCOHOL (UNII: LKG8494WBH) PANTHENOL (UNII: WV9CM0O67Z) ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I) DOCOSANOL (UNII: 9G1OE216XY) STEARETH-2 (UNII: V56DFE46J5) STEARETH-21 (UNII: 53J3F32P58) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CHLORPHENESIN (UNII: I670DAL4SZ) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) MICA (UNII: V8A1AW0880) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72288-338-26 1 in 1 CARTON 04/26/2018 1 188 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/26/2018 Labeler - Amazon.com Services LLC (128990418) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(72288-338)