Label: EXUVIANCE AGE REVERSE DAY REPAIR WITH SUNSCREEN BROAD SPECTRUM SPF 30- avobenzone, octinoxate, and octisalate cream
- NDC Code(s): 58414-0023-1
- Packager: NeoStrata Company Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 10, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
-
Uses
- Helps prevent sunburn
- If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
- Warnings
-
Directions
- Apply liberally to face and neck daily following cleansing, 15 minutes before sun exposure
- Use a water resistant sunscreen if swimming or sweating
- Reapply at least every 2 hours
-
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 am – 2 pm
- Wear long-sleeved shirts, pants, hats and sunglasses
- Children under 6 months: Ask a doctor
- Other information
-
Inactive ingredients
Water, Acetyl Glucosamine, Butyloctyl Salicylate, Cyclopentasiloxane, Glyceryl Stearate, Butylene Glycol, Butyrospermum Parkii (Shea) Butter, PEG-100 Stearate, Dimethicone, Cetyl Alcohol, Nylon-12, Triacontanyl PVP, Retinol, Citric Acid, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, Coffea Arabica (Coffee) Fruit Extract, Tocopheryl Acetate, Rosa Damascena Flower Oil, Punica Granatum Extract, Arginine, Glycerin, Propylene Glycol, Cyclohexasiloxane, Caprylyl Glycol, Dimethiconol, Disodium EDTA, BHT, Xanthan Gum, PEG-75 Stearate, Ceteth-20, Steareth-20, Polysorbate 20, Triethyl Citrate, Ammonium Acryloyldimethyltaurate/VP Copolymer, Methyldihydrojasmonate, Carbomer, Ethylene Brassylate, Phenoxyethanol, Chlorphenesin, Yellow 5 (CI 19140), Red 33 (CI 17200).
- Questions or comments?
- PRINCIPAL DISPLAY PANEL - 50 g Tube Carton
-
INGREDIENTS AND APPEARANCE
EXUVIANCE AGE REVERSE DAY REPAIR WITH SUNSCREEN BROAD SPECTRUM SPF 30
avobenzone, octinoxate, and octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58414-0023 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 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) N-ACETYLGLUCOSAMINE (UNII: V956696549) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SHEA BUTTER (UNII: K49155WL9Y) PEG-100 STEARATE (UNII: YD01N1999R) DIMETHICONE (UNII: 92RU3N3Y1O) CETYL ALCOHOL (UNII: 936JST6JCN) NYLON-12 (UNII: 446U8J075B) TRICONTANYL POVIDONE (UNII: N0SS3Q238D) RETINOL (UNII: G2SH0XKK91) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) COFFEA ARABICA FRUIT (UNII: HOX6BEK27Q) ROSA X DAMASCENA FLOWER OIL (UNII: 18920M3T13) ARGININE (UNII: 94ZLA3W45F) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) CYCLOMETHICONE 6 (UNII: XHK3U310BA) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) PEG-75 STEARATE (UNII: OT38R0N74H) CETETH-20 (UNII: I835H2IHHX) STEARETH-20 (UNII: L0Q8IK9E08) DIMETHICONOL (100000 CST) (UNII: OSA9UP217S) POLYSORBATE 20 (UNII: 7T1F30V5YH) XANTHAN GUM (UNII: TTV12P4NEE) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD) CHLORPHENESIN (UNII: I670DAL4SZ) PHENOXYETHANOL (UNII: HIE492ZZ3T) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58414-0023-1 1 in 1 CARTON 10/01/2019 1 50 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 Drug M020 10/01/2019 Labeler - NeoStrata Company Inc. (605754829)
