NDC 62802-183 Ocean Potion Quick Dry Kids 50 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 62802-183?
What are the uses for Ocean Potion Quick Dry Kids 50 Sunscreen?
Which are Ocean Potion Quick Dry Kids 50 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Ocean Potion Quick Dry Kids 50 Sunscreen 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)
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 1G56KV7BUJ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYPROMELLOSE 2208 (15000 MPA.S) (UNII: Z78RG6M2N2)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
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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".