NDC 61979-002 Body Time Sun Broad Spectrum Spf30 Anti-aging Day
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61979 - Bela Vida Holdings, Llc Dba Body Time
- 61979-002 - Body Time Sun Broad Spectrum Spf30 Anti-aging Day
Product Packages
NDC Code 61979-002-59
Package Description: 1 JAR in 1 BOX / 59 mL in 1 JAR
Product Details
What is NDC 61979-002?
What are the uses for Body Time Sun Broad Spectrum Spf30 Anti-aging Day?
Which are Body Time Sun Broad Spectrum Spf30 Anti-aging Day UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Body Time Sun Broad Spectrum Spf30 Anti-aging Day 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)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- ISOEICOSANE (UNII: AR294KAG3T)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- GLYCERIN (UNII: PDC6A3C0OX)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- HYDROXYMETHYL CELLULOSE (UNII: 273FM27VK1)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- POMEGRANATE (UNII: 56687D1Z4D)
* 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".