NDC 76398-001 Illuminating Protective Primer Spf 12
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 76398-001?
Which are Illuminating Protective Primer Spf 12 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Illuminating Protective Primer Spf 12 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- SHEA BUTTER (UNII: K49155WL9Y)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- EPILOBIUM ANGUSTIFOLIUM LEAF (UNII: 7NV86426N2)
- VANILLA (UNII: Q74T35078H)
- DIPTERYX ODORATA SEED (UNII: D43A5L1U6L)
- SAPINDUS MUKOROSSI FRUIT (UNII: 66H9NW427Y)
- COCONUT OIL (UNII: Q9L0O73W7L)
- PATCHOULI OIL (UNII: F3IN55X5PO)
- CANANGA OIL (UNII: 8YOY78GNNX)
- AMYRIS BALSAMIFERA OIL (UNII: I1BJ961J2E)
- VETIVER OIL (UNII: 9M9P32M01L)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- CAFFEINE (UNII: 3G6A5W338E)
- CAESALPINIA SPINOSA RESIN (UNII: WL3883U2PO)
- PROPYLENE GLYCOL LAURATES (UNII: 40KT317HGP)
- SQUALANE (UNII: GW89575KF9)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MICA (UNII: V8A1AW0880)
* Please review the disclaimer below.
[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".