NDC 59735-100 Bo Spf15
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What is NDC 59735-100?
What are the uses for Bo Spf15?
Which are Bo Spf15 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)
Which are Bo Spf15 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SHEA BUTTER (UNII: K49155WL9Y)
- COCOA BUTTER (UNII: 512OYT1CRR)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- COCO-GLYCERIDES (UNII: ISE9I7DNUG)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- CRAMBE HISPANICA SUBSP. ABYSSINICA SEED OIL (UNII: 0QW9S92J3K)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PANTHENOL (UNII: WV9CM0O67Z)
- NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM PALMITOYL PROLINE (UNII: 64L053FRFO)
- CETETH-20 (UNII: I835H2IHHX)
- PEG-75 STEARATE (UNII: OT38R0N74H)
- SODIUM OLEATE (UNII: 399SL044HN)
- STEARETH-20 (UNII: L0Q8IK9E08)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- O-CYMEN-5-OL (UNII: H41B6Q1I9L)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
* 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".