NDC 68807-319 Advanced Marine Biology Day Spf 20 La Prairie Group Ag
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What is NDC 68807-319?
What are the uses for Advanced Marine Biology Day Spf 20 La Prairie Group Ag?
Which are Advanced Marine Biology Day Spf 20 La Prairie Group Ag 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)
Which are Advanced Marine Biology Day Spf 20 La Prairie Group Ag 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)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- SHEA BUTTER (UNII: K49155WL9Y)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PANTHENOL (UNII: WV9CM0O67Z)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DULSE (UNII: 7832HOY4ZQ)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- LIMONIUM GERBERI FLOWERING TOP (UNII: V4O4C05BJ2)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIPROPYLENE GLYCOL DIBENZOATE (UNII: 6OA5ZDY41O)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- PPG-15 STEARYL ETHER BENZOATE (UNII: 80D2J6361M)
- CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SORBIC ACID (UNII: X045WJ989B)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
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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".