NDC 59062-5400 Outdoor Essentials
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 59062-5400?
What are the uses for Outdoor Essentials?
Which are Outdoor Essentials UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Outdoor Essentials 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- STEARYL/OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: PN88NW0KPK)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
- LAPONITE (UNII: D703131383)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SQUALANE (UNII: GW89575KF9)
- TOMATO SEED OIL (UNII: 7N87T9C06T)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CRANBERRY SEED OIL (UNII: 73KDS3BW5E)
- RASPBERRY SEED OIL (UNII: 9S8867952A)
- NIGELLA SATIVA SEED OIL (UNII: CS4U38E731)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
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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".