Label: PURLISSE BLUE LOTUS DAILY MOISTURIZER SPF 30- avobenzone, homosalate, octisalate, octocrylene lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 72407-401-11 - Packager: Pur-Lisse Beauty, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 January 17, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- Purpose
- Use
- Warnings
- KEEP OUT OF REACH OF CHILDREN
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Directions
FOR SUNSCREEN USE:
- APPLY LIBERALLY 15 MINUTES 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 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. TO 2 P.M.
- WEAR LONG-SLEEVED SHIRTS, PANTS, HATS AND SUNGLASSES
- CHILDREN UNDER 6 MONTHS OF AGE: ASK A DOCTOR
- Other information
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Inactive ingredients
Water, Glycerin, Cetearyl Alcohol, Dimethicone, Cyclopentasiloxane, Tocopheryl Acetate, Hydrolyzed Lupine Protein Octenylsuccinate, Aphanizomenon Flos Aquae Extract, Hydrolyzed Soy Protein, Camellia Sinensis Leaf Extract, Nymphaea Coerulea Flower Extract, Sodium Hyaluronate, Dipotassium Glycyrrhizate, Dicetyl Phosphate, Ceteth-10 Phosphate, Aminomethyl Propanol, Carbomer, Disodium EDTA, Chlorphenesin, Caprylyl Glycol, Phenoxyethanol, Fragrance
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PURLISSE BLUE LOTUS DAILY MOISTURIZER SPF 30
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72407-401 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.2 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 13.2 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 8.8 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE (UNII: 92RU3N3Y1O) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) HYDROLYZED LUPINUS ALBUS SEED PROTEIN (ENZYMATIC; 3500 MW) (UNII: K3A2RS79IG) APHANIZOMENON FLOSAQUAE (UNII: 49VG1X560X) HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6) GREEN TEA LEAF (UNII: W2ZU1RY8B0) NYMPHAEA CAERULEA FLOWER (UNII: S9560USZ74) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) EDETATE DISODIUM (UNII: 7FLD91C86K) CHLORPHENESIN (UNII: I670DAL4SZ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72407-401-11 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 04/15/2020 Labeler - Pur-Lisse Beauty, LLC (080593370)
