Label: ETHYLHEXYL METHOXYCINNAMATE CREAM- detoxifying day cream rich cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70493-521-01, 70493-521-02 - Packager: inspira:cosmetics GmbH
- 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 October 13, 2022
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INACTIVE INGREDIENT
Aqua [water], butylene glycol, glycerin, isostearyl isostearate, ethylhexyl methoxycinnamate, glyceryl stearate citrate, cetearyl alcohol, caprylic/capric triglyceride, propylheptyl caprylate, polyglyceryl-3 stearate, glyceryl, stearate, pentylene glycol, butyrospermum parkii (shea) butter, hydrogenated, coco-glycerides, hydrogenated vegetable oil, 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, lecithin, sorbitan oleate, sodium levulinate, ascorbyl palmitate, BHT, tocopherol, tetrasodium glutamate, diacetate, citric acid, sodium citrate, sodium hydroxide, sodium anisate, geraniol, phenoxyethanol, sodium benzoate, potassium sorbate
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Active Ingredients information and purpose
ETHYLHEXYL METHOXYCINNAMATE Cream for UV and IR protection
Rich day care cream providing UV and IR protection for stressed and dry 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. -
INGREDIENTS AND APPEARANCE
ETHYLHEXYL METHOXYCINNAMATE CREAM
detoxifying day cream rich creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70493-521 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 2 g in 50 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERIN (UNII: PDC6A3C0OX) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) PHENOXYETHANOL (UNII: HIE492ZZ3T) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4) CAMELLIA JAPONICA FLOWER (UNII: KUB8101TNF) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0) EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) HYDROGENATED COCO-GLYCERIDES (UNII: XDD37N2GPR) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) PENTYLENE GLYCOL (UNII: 50C1307PZG) SHEA BUTTER (UNII: K49155WL9Y) DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20) LEONTOPODIUM ALPINUM FLOWERING TOP (UNII: QQC1AK06RK) ALLANTOIN, (+)- (UNII: XDK458E1J9) BISABOLOL OXIDE B, (-)- (UNII: S32G48306Y) THERMUS THERMOPHILUS LYSATE (UNII: 775R692494) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) POLYISOBUTYLENE (1300 MW) (UNII: 241BN7J12Y) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) TOCOPHEROL (UNII: R0ZB2556P8) TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM CITRATE (UNII: 1Q73Q2JULR) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM ANISATE (UNII: F9WFJ28MV9) GERANIOL (UNII: L837108USY) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CAPRYLIC/CAPRIC/PALMITIC/STEARIC TRIGLYCERIDE (UNII: ZF29F7IK5I) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) WATER (UNII: 059QF0KO0R) ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y) PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD) POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91) PROPANEDIOL (UNII: 5965N8W85T) HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ) SACCHARIDE ISOMERATE (UNII: W8K377W98I) SODIUM LEVULINATE (UNII: VK44E1MQU8) ASCORBYL PALMITATE (UNII: QN83US2B0N) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70493-521-02 1 in 1 BOX 02/01/2016 1 NDC:70493-521-01 50 mL in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 02/01/2016 Labeler - inspira:cosmetics GmbH (329455898) Registrant - inspira:cosmetics GmbH (329455898) Establishment Name Address ID/FEI Business Operations inspira: cosmetics GmbH 329455898 manufacture(70493-521)