NDC 75870-002 Soft Derm Intensive Defense 8 Spf
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 75870-002?
Which are Soft Derm Intensive Defense 8 Spf UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM (UNII: D1JT611TNE) (Active Moiety)
Which are Soft Derm Intensive Defense 8 Spf 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:
- OCTYLDODECYL MYRISTATE (UNII: S013N99GR8)
- PEG-6 STEARATE (UNII: 8LQC57C6B0)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAPER BERRY (UNII: 7G4C45EE8C)
- CAPSOSIPHON FULVESCENS (UNII: C59NK6GFJH)
- CETETH-20 (UNII: I835H2IHHX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- STEARETH-20 (UNII: L0Q8IK9E08)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALLANTOIN (UNII: 344S277G0Z)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- HYDROXYSTEARIC ACID (UNII: 933ANU3H2S)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- WATER (UNII: 059QF0KO0R)
- ULVA COMPRESSA PROTEIN (ACID HYDROLYZED, 300-5000 MW) (UNII: Q04O53779D)
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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".