FDA.reportPublic FDA data

Multi Effect Day Cream SPF 25

Manufacturer
Sano International Ltd. | Peer Pharma Ltd.
Effective date
2017-11-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:52:59

Label at a glance#

ProductMulti Effect Day Cream SPF 25
Active ingredientOCTOCRYLENE, OCTISALATE, AVOBENZONE, HOMOSALATE, OCTINOXATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Multi Effect Day CreamMulti Effect Day Cream

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7%

Octocrylene 5%

Octisalate 5%

Avobenzone 3%

Homosalate 2%

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PURPOSE SECTION

Provides SPF 25 protection

INDICATIONS & USAGE SECTION

To Use: Smooth onto face.
For Sunscreen Use: Apply liberally 15 minutes before sun exposure. 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 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-sleeve shirts, pants, hats, and sunglasses.

WARNINGS SECTION

DOSAGE & ADMINISTRATION SECTION

Smooth on to face.

INACTIVE INGREDIENT SECTION

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69435-1701-12020-01-31C16284748780-19d75b9cf-eb10-f424-e053-dadaa90a57ceMulti Effect Day Cream SPF 25

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69435-1701-1Multi Effect Day Cream SPF 2550 mL in 1 CONTAINERCREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69435-1701MULTI EFFECT DAY CREAM SPF 25 (OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, HOMOSALATE) CREAM [SANO INTERNATIONAL LTD.]2Legacy NDC, 1 package rows20171116_50afd836-72c1-36be-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69435-170169435-1701-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 matching rows.

Name, UNII, Kind table
NameUNIIKind
JOJOBA OIL724GKU717MIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ALMOND OIL66YXD4DKO9IACT
DMDM HYDANTOINBYR0546TOWIACT
ALLANTOIN344S277G0ZIACT
CHLORPHENESINI670DAL4SZIACT
HYALURONATE SODIUMYSE9PPT4THIACT
ASCORBYL TETRAISOPALMITATE47143LT58AIACT
ISOHEXADECANE918X1OUF1EIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CETEARYL GLUCOSIDE09FUA47KNAIACT
CYCLOMETHICONE 50THT5PCI0RIACT
GLYCERINPDC6A3C0OXIACT
PUNICA GRANATUM ROOT BARKCLV24I3T1DIACT
SHEA BUTTERK49155WL9YIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
NIACINAMIDE25X51I8RD4IACT
DIMETHICONE92RU3N3Y1OIACT
SEA SALT87GE52P74GIACT
ALOE VERA LEAFZY81Z83H0XIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PANTHENOLWV9CM0O67ZIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CHAMAEMELUM NOBILE FLOWERO2T154T6OGIACT
AVOCADO OIL6VNO72PFC1IACT
WATER059QF0KO0RIACT
OCTOCRYLENE5A68WGF6WMACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTINOXATE4Y5P7MUD51ACTIB
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATEANQ870JD20IACT

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
5e1a757c-35a2-5be1-e053-2a91aa0a81fa50afd836-72c1-36be-e054-00144ff88e882017-11-16Exact identifier
spl id: 5e1a757c-35a2-5be1-e053-2a91aa0a81fa
spl set id: 50afd836-72c1-36be-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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