NDC 75870-001 Lift Therapy Force Lift Day 20 Spf
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 75870-001?
Which are Lift Therapy Force Lift Day 20 Spf UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Lift Therapy Force Lift Day 20 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- TRIBEHENIN PEG-20 ESTERS (UNII: 84K9EH29Y9)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALCOHOL (UNII: 3K9958V90M)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SOY ISOFLAVONES (UNII: 71B37NR06D)
- ACMELLA OLERACEA FLOWER (UNII: 2794N5KM0K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- POLYAMINOPROPYL BIGUANIDE (UNII: 322U039GMF)
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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".