NDC 40046-0030 Tendertone Lip Balm Spf 12
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 40046-0030?
Which are Tendertone Lip Balm Spf 12 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)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Tendertone Lip Balm 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:
- PETROLATUM (UNII: 4T6H12BN9U)
- ASTROCARYUM MURUMURU SEED BUTTER (UNII: 12V64UPU6R)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- BLACK OLIVE (UNII: 2M6QWV94OC)
- WHEAT BRAN (UNII: 6L966A1IMR)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- OLEIC ACID (UNII: 2UMI9U37CP)
- PALMITIC ACID (UNII: 2V16EO95H1)
- POTASSIUM SULFATE (UNII: 1K573LC5TV)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- COCHINEAL (UNII: TZ8Z31B35M)
- 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)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
* 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".