NDC 47124-449 Sport Sunscreen Spf 50 Wegmans
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 47124-449?
What are the uses for Sport Sunscreen Spf 50 Wegmans?
Which are Sport Sunscreen Spf 50 Wegmans UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Sport Sunscreen Spf 50 Wegmans 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:
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- ALOE (UNII: V5VD430YW9)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CERESIN (UNII: Q1LS2UJO3A)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- MINERAL OIL (UNII: T5L8T28FGP)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
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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".