NDC 72484-202 Rory Broad Spectrum Spf 28 Sunscreen Face Moisturizer
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 72484-202?
What are the uses for Rory Broad Spectrum Spf 28 Sunscreen Face Moisturizer?
Which are Rory Broad Spectrum Spf 28 Sunscreen Face Moisturizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Rory Broad Spectrum Spf 28 Sunscreen Face Moisturizer Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- POLYGONUM AVICULARE WHOLE (UNII: M990N03611)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- COCONUT OIL (UNII: Q9L0O73W7L)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL DIMETHICONE 150 (UNII: 5L694Y0T22)
- ISOCETYL STEARATE (UNII: 3RJ7186O9W)
- WATER (UNII: 059QF0KO0R)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- VACCINIUM VITIS-IDAEA FRUIT OIL (UNII: 16Y54799WZ)
- LEPIDIUM SATIVUM WHOLE (UNII: 0FL88F2R2Q)
- SORBITOL (UNII: 506T60A25R)
- ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- XANTHAN GUM (UNII: TTV12P4NEE)
- VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
- QUERCUS SUBER BARK (UNII: 8R5219271Q)
- OCTISALATE (UNII: 4X49Y0596W)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- CALCIUM GLUCONATE (UNII: SQE6VB453K)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- VITIS VINIFERA FRUIT OIL (UNII: YQ5Q4Y2Z8U)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ISOMALT (UNII: S870P55O2W)
- VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- QUERCUS SPP. WHOLE (UNII: MF4E5I2OUQ)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".