Label: PLIUS DAILY SPF MOISTURIZER SPF 30- avobenzone, octisalate, octocrylene cream
- NDC Code(s): 80573-089-30
- Packager: PLIUS, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
-
Directions
- Apply liberally 15 minutes before sun exposure
- Children under 6 months of age: ask a doctor
- Reapply at least every 2 hours
- Reapply as needed or after towel drying, swimming, or sweating
- Use a water-resistant sunscreen if swimming or sweating
- Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures including: Sun Protection Measures.
- Limit time in the sun, especially from 10 am. - 2 p.m.
- Wear long-sleeved shirts, pants, hats, and sunglasses
-
Inactive ingredients
Acrylates Copolymer, Aloe Barbadensis Leaf (Aloe Vera Ge) Juice, Aqua(Deionized Water), Ascorbyl Palmitate (Vitamin C), Butyloctyl Salicylate Camellia Sinensis (Green Tea) Extract, Caprylic/Capric Triglyceride, Cetearyl Olivate, Cetyl Alcohol, Cyclopentasiloxane, Cyclotetrasiloxane, Daucus Carota Sativa (Carrot) Extract, Dimethicone, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Hyaluronic Acid, Magnesium Aluminum Silicate, Phenoxyethanol, Polysorbate-20, Saccharide Isomerate, Sodium Hydroxide, Sorbitan Olivate, Stearyl Alcohol, Tocopheryl Acetate (Vitamin E)
- Other Information:
- Questions?
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
PLIUS DAILY SPF MOISTURIZER SPF 30
avobenzone, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80573-089 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 OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 80 mg in 1 mL Inactive Ingredients Ingredient Name Strength BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ASCORBYL PALMITATE (UNII: QN83US2B0N) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) GREEN TEA LEAF (UNII: W2ZU1RY8B0) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETEARYL OLIVATE (UNII: 58B69Q84JO) CETYL ALCOHOL (UNII: 936JST6JCN) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CYCLOMETHICONE 4 (UNII: CZ227117JE) CARROT (UNII: L56Z1JK48B) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) SUNFLOWER OIL (UNII: 3W1JG795YI) HYALURONIC ACID (UNII: S270N0TRQY) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) SACCHARIDE ISOMERATE (UNII: W8K377W98I) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITAN OLIVATE (UNII: MDL271E3GR) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80573-089-30 1 in 1 CARTON 09/14/2020 1 30 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 Drug M020 09/14/2020 Labeler - PLIUS, Inc (117647046)
