NDC 53675-100 Aruba Aloe Island Remedy Daily Ultra Aloe
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What is NDC 53675-100?
What are the uses for Aruba Aloe Island Remedy Daily Ultra Aloe?
Which are Aruba Aloe Island Remedy Daily Ultra Aloe UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Aruba Aloe Island Remedy Daily Ultra Aloe 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CETEARYL ISONONANOATE (UNII: P5O01U99NI)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- EQUISETUM HYEMALE (UNII: 59677RXH25)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- PRUNUS SEROTINA BARK (UNII: 5D48E975HA)
- CLOVE (UNII: K48IKT5321)
- DECYL OLEATE (UNII: ZGR06DO97T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- TROLAMINE (UNII: 9O3K93S3TK)
- JOJOBA OIL (UNII: 724GKU717M)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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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".