NDC 57913-2834 R.e.m. Day Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 57913-2834?
What are the uses for R.e.m. Day Spf 30?
Which are R.e.m. Day Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are R.e.m. Day Spf 30 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:
- WATER (UNII: 059QF0KO0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- LEVOMENOL (UNII: 24WE03BX2T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- EUROPEAN HAZELNUT OIL (UNII: 8RQ2839AVG)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- SESAME OIL (UNII: QX10HYY4QV)
- HYDNOCARPUS KURZII SEED OIL (UNII: N757YEZ18Q)
- JOJOBA OIL (UNII: 724GKU717M)
- GINKGO (UNII: 19FUJ2C58T)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- STEARETH-20 (UNII: L0Q8IK9E08)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- O-CYMEN-5-OL (UNII: H41B6Q1I9L)
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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".