NDC 58443-0256 Miami Beach Kids Sunscreen Broad Spectrum Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises Inc.
- 58443-0256 - Miami Beach
Product Characteristics
Product Packages
NDC Code 58443-0256-4
Package Description: 177 mL in 1 BOTTLE
Product Details
What is NDC 58443-0256?
What are the uses for Miami Beach Kids Sunscreen Broad Spectrum Spf 50?
Which are Miami Beach Kids Sunscreen Broad Spectrum Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Miami Beach Kids Sunscreen Broad Spectrum Spf 50 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:
- COCOA BUTTER (UNII: 512OYT1CRR)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- CARBOMER 1342 (UNII: 809Y72KV36)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETIC ACID (UNII: 9G34HU7RV0)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- CORN OIL (UNII: 8470G57WFM)
- .BETA.-CAROTENE (UNII: 01YAE03M7J)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)
- APRICOT KERNEL OIL (UNII: 54JB35T06A)
- SOLANUM LYCOPERSICUM FRUITING TOP (UNII: X636CG4BH0)
- ROSEMARY (UNII: IJ67X351P9)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
* 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".