Label: CVS BEAUTY 360 7-IN-1 COMPLETE DAILY MOISTURIZER ANTI-AGING FORMULA WITH BROAD SPECTRUM SPF 15 SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene lotion
- NDC Code(s): 51316-049-01, 51316-049-17
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 April 26, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
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Directions
• apply liberally 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 a.m. - 2 p.m.
• wear long-sleeved shirts, pants, hats, and sunglasses• children under 6 months: Ask a doctor
- Other information
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Inactive ingredients
WATER, GLYCERIN, CETEARYL ALCOHOL, SUCROSE DILAURATE, PISUM SATIVUM (PEA) EXTRACT, BUTYLENE GLYCOL, PALMITOYL OLIGOPEPTIDE, PALMITOYL TETRAPEPTIDE-7, POLYETHYLENE, DIMETHICONE, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, PENTYLENE GLYCOL, ASCORBIC ACID, CAMELLIA SINENSIS LEAF EXTRACT, STEARYL ALCOHOL, ISOHEXADECANE, CETYL ALCOHOL, PANTHENOL, TOCOPHERYL ACETATE, BEHENYL ALCOHOL, DIMETHICONOL, CETEARYL GLUCOSIDE, PEG-100 STEARATE, DISODIUM EDTA, STEARIC ACID, BHT, POLYSORBATE 60, CAPRYLYL GLYCOL, PHENOXYETHANOL, HEXYLENE GLYCOL, TRIETHANOLAMINE, CITRIC ACID, CARBOMER, POLYSORBATE-20, TITANIUM DIOXIDE.
- Label
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INGREDIENTS AND APPEARANCE
CVS BEAUTY 360 7-IN-1 COMPLETE DAILY MOISTURIZER ANTI-AGING FORMULA WITH BROAD SPECTRUM SPF 15 SUNSCREEN
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51316-049 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 HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 40 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 26 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 45 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE (UNII: 92RU3N3Y1O) PEG-100 STEARATE (UNII: YD01N1999R) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) DOCOSANOL (UNII: 9G1OE216XY) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) DIMETHICONOL (100000 CST) (UNII: OSA9UP217S) PANTHENOL (UNII: WV9CM0O67Z) GLYCERIN (UNII: PDC6A3C0OX) ISOHEXADECANE (UNII: 918X1OUF1E) SUCROSE DILAURATE (UNII: 5926LC4S7M) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) POLYSORBATE 20 (UNII: 7T1F30V5YH) CETYL ALCOHOL (UNII: 936JST6JCN) STEARIC ACID (UNII: 4ELV7Z65AP) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) PENTYLENE GLYCOL (UNII: 50C1307PZG) PEA (UNII: W4X7H8GYFM) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) EDETATE DISODIUM (UNII: 7FLD91C86K) ASCORBIC ACID (UNII: PQ6CK8PD0R) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) POLYSORBATE 60 (UNII: CAL22UVI4M) TROLAMINE (UNII: 9O3K93S3TK) CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17) HEXYLENE GLYCOL (UNII: KEH0A3F75J) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51316-049-01 1 in 1 BOX 06/13/2018 1 NDC:51316-049-17 50 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 M020 06/13/2018 Labeler - CVS Pharmacy (062312574)