NDC 69000-018 Shell Future Resist Foundation Broad Spectrum Spf 20 Delilah
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What is NDC 69000-018?
What are the uses for Shell Future Resist Foundation Broad Spectrum Spf 20 Delilah?
Which are Shell Future Resist Foundation Broad Spectrum Spf 20 Delilah UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Shell Future Resist Foundation Broad Spectrum Spf 20 Delilah 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)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TROPOLONE (UNII: 7L6DL16P1T)
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".