NDC 40046-0041 Tinted Lip Conditioner Spf 15 Plus Lavender
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 40046-0041?
Which are Tinted Lip Conditioner Spf 15 Plus Lavender UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Tinted Lip Conditioner Spf 15 Plus Lavender 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:
- PETROLATUM (UNII: 4T6H12BN9U)
- CASTOR OIL (UNII: D5340Y2I9G)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYISOBUTYLENE (35000 MW) (UNII: 98553S1MHQ)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ALMOND OIL (UNII: 66YXD4DKO9)
- SHEA BUTTER (UNII: K49155WL9Y)
- ASTROCARYUM MURUMURU SEED BUTTER (UNII: 12V64UPU6R)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- WHEAT GERM OIL (UNII: 14C97E680P)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- OCTYLTRIETHOXYSILANE (UNII: LDC331P08E)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- SACCHARIN (UNII: FST467XS7D)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- D&C RED NO. 6 (UNII: 481744AI4O)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- 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".