FDA.reportPublic FDA data

PURLISSE BLUE LOTUS DAILY MOISTURIZER

Manufacturer
Pur-Lisse Beauty, LLC
Effective date
2022-01-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:47:05

Label at a glance#

ProductPURLISSE BLUE LOTUS DAILY MOISTURIZER SPF 30
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure9 sections

Dosage and administration

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 TIM...

Storage and handling

PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN LIGHT.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

AVOBENZONE  2.2%

HOMOSALATE  13.2%

OCTISALATE  5%

OCTOCRYLENE  8.8%

Purpose

OTC - PURPOSE SECTION

SUNSCREEN

Use

INDICATIONS & USAGE SECTION

USE TO HELP PREVENT SUNBURN

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

DO NOT USE ON DAMAGED OR BROKEN SKIN.

WHEN USING THIS PRODUCTKEEP OUT OF EYES. RINSE WITH WATER TO REMOVE.

STOP USE AND ASK A DOCTOR IF RASH OCCURS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN LIGHT.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b UC_Blue Lotus Daily Moisturizer SPF-3001b UC_Blue Lotus Daily Moisturizer SPF-30

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72407-401-112024-01-30C16284748780-11030e365-2062-111a-e063-dadaa90a10e2PURLISSE BLUE LOTUS DAILY MOISTURIZER WITH SPF 30 SUNSCREEN (72407-401)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72407-401-11PURLISSE BLUE LOTUS DAILY MOISTURIZERSPF 3050 mL in 1 BOTTLELOTION504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72407-401PURLISSE BLUE LOTUS DAILY MOISTURIZER SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [PUR-LISSE BEAUTY, LLC]4Legacy NDC, 1 package rows20220118_1c8ec9c9-7984-47dd-8972-d728fdec9af5.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72407-40172407-401-11

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
DIMETHICONE92RU3N3Y1OIACT
CYCLOMETHICONE 50THT5PCI0RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
HYDROLYZED LUPINUS ALBUS SEED PROTEIN (ENZYMATIC; 3500 MW)K3A2RS79IGIACT
APHANIZOMENON FLOSAQUAE49VG1X560XIACT
HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW)1394NXB9L6IACT
GREEN TEA LEAFW2ZU1RY8B0IACT
NYMPHAEA CAERULEA FLOWERS9560USZ74IACT
HYALURONATE SODIUMYSE9PPT4THIACT
GLYCYRRHIZINATE DIPOTASSIUMCA2Y0FE3FXIACT
DIHEXADECYL PHOSPHATE2V6E5WN99NIACT
CETETH-10 PHOSPHATE4E05O5N49GIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
EDETATE DISODIUM7FLD91C86KIACT
CHLORPHENESINI670DAL4SZIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d5d21fcf-0ef2-b187-e053-2a95a90a3abb1c8ec9c9-7984-47dd-8972-d728fdec9af52022-01-17WarningsExact identifier
spl id: d5d21fcf-0ef2-b187-e053-2a95a90a3abb
spl set id: 1c8ec9c9-7984-47dd-8972-d728fdec9af5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.