FDA.reportPublic FDA data

ETHYLHEXYL METHOXYCINNAMATE Cream

Manufacturer
inspira: cosmeticsGmbH | inspira: cosmetics GmbH
Effective date
2022-10-13
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:51:40

Label at a glance#

ProductETHYLHEXYL METHOXYCINNAMATE Cream
Active ingredientOCTINOXATE
Label structure3 sections

Dosage and administration

Directions: Every morning, after cleansing evenly spread a small amount of cream over your face, neck and the area above your neckline and gently rub it in. Avoid the skin around your eyes.

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Aqua [water], methyl glucose sesquistearate, butylene glycol, glycerin, caprylic/capric triglyceride, propylheptyl, caprylate, glyceryl stearate, cetearyl alcohol, pentylene glycol, silica, ethylhexyl triazone, diethylamino hydroxybenzoyl hexyl benzoate, propanediol, hydrogenated, polyisobutene, leontopodium alpinum flower/leaf extract, sodium hyaluronate,allantoin, bisabolol, thermus thermophillus ferment, camellia japonica flower extract, glyceryl caprylate, saccharide isomerate, polyisobutene, sodium acrylate/sodium, acryloyldimethyl taurate copolymer, caprylyl/capryl glucoside, sodium stearoyl, lactylate, sorbitan oleate, lecithin, ascorbyl palmitate, BHT, tocopherol, tetrasodium, glutamate diacetate, citric acid, sodium citrate, sodium hydroxide, phenoxyethanol, sodium benzoate, potassium sorbate

Directions

OTC - WHEN USING SECTION

Directions: Every morning, after cleansing evenly spread a small amount of cream over your face, neck and the area above your neckline and gently rub it in.

Avoid the skin around your eyes.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ETHYLHEXYL METHOXYCINNAMATE Cream for UV and IR Protection

Day care cream providing UV and IR protection for oily and combination skin.High-alpine edelweiss combats premature ageing and aggressive environmental influences, while a special active substance with a detoxifying effect purifies the skin and hyaluronic acid and PentavitinTM* smoothe it.

Outside PackagingOutside Packaging

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70493-520-022024-08-08C16284748780-19d75b9d0-5f3e-f424-e053-dadaa90a57ceDetoxifying Day Cream Regular
70493-520-022024-01-30C16284748780-19d75b9d0-5f3e-f424-e053-dadaa90a57ceDetoxifying Day Cream Regular
70493-520-022022-10-13C16284748780-19d75b9d0-5f3e-f424-e053-dadaa90a57ceDetoxifying Day Cream Regular
70493-520-022020-01-31C16284748780-19d75b9d0-5f3e-f424-e053-dadaa90a57ceDetoxifying Day Cream Regular

Products#

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

DailyMed product names page 1 of 1 · 40 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70493-52070493-520-01, 70493-520-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMELLIA JAPONICA FLOWERKUB8101TNFIACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
SACCHARIDE ISOMERATEW8K377W98IIACT
POLYISOBUTYLENE (1300 MW)241BN7J12YIACT
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW)1DXE3F3OZXIACT
CAPRYLYL/CAPRYL OLIGOGLUCOSIDEE00JL9G9K0IACT
SODIUM STEAROYL LACTYLATEIN99IT31LNIACT
SORBITAN MONOOLEATE06XEA2VD56IACT
ASCORBYL PALMITATEQN83US2B0NIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
TOCOPHEROLR0ZB2556P8IACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
SODIUM CITRATE1Q73Q2JULRIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM BENZOATEOJ245FE5EUIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
PROPYLHEPTYL CAPRYLATE991Z19V2ODIACT
HYDROGENATED POLYBUTENE (1300 MW)7D1YQ9Y5EZIACT
ALLANTOIN344S277G0ZIACT
THERMUS THERMOPHILUS LYSATE775R692494IACT
PEG-120 GLYCERYL STEARATE6941286E4IIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
WATER059QF0KO0RIACT
METHYL GLUCOSE SESQUISTEARATEV1YW10H14DIACT
GLYCERINPDC6A3C0OXIACT
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDEFJ1H6M2JG9IACT
PENTYLENE GLYCOL50C1307PZGIACT
HYDRATED SILICAY6O7T4G8P9IACT
LEONTOPODIUM ALPINUM FLOWERING TOPQQC1AK06RKIACT
OCTINOXATE4Y5P7MUD51ACTIB
ETHYLHEXYL TRIAZONEXQN8R9SAK4IACT
PROPANEDIOL5965N8W85TIACT
HYALURONATE SODIUMYSE9PPT4THIACT
SODIUM HYDROXIDE55X04QC32IIACT
LEVOMENOL24WE03BX2TIACT
EGG PHOSPHOLIPIDS1Z74184RGVIACT
CITRIC ACID ACETATEDSO12WL7AUIACT
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
1f1d623f-272e-abba-e063-6394a90a04a02c7c8d54-28c1-0179-e054-00144ff8d46c2024-08-07Exact identifier
spl set id: 2c7c8d54-28c1-0179-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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