NDC 58418-223 Skin Crave Spf30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 58418-223-01
Package Description: 30 mL in 1 BOTTLE
NDC Code 58418-223-02
Package Description: 60 mL in 1 BOTTLE
NDC Code 58418-223-04
Package Description: 120 mL in 1 BOTTLE
NDC Code 58418-223-08
Package Description: 240 mL in 1 BOTTLE
NDC Code 58418-223-10
Package Description: 10 mL in 1 BOTTLE, SPRAY
NDC Code 58418-223-12
Package Description: 360 mL in 1 BOTTLE, PUMP
NDC Code 58418-223-16
Package Description: 480 mL in 1 BOTTLE, PUMP
NDC Code 58418-223-28
Package Description: 3840 mL in 1 BOTTLE, PUMP
NDC Code 58418-223-64
Package Description: 1920 mL in 1 BOTTLE, PUMP
NDC Code 58418-223-80
Package Description: 240 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 58418-223?
What are the uses for Skin Crave Spf30 Sunscreen?
Which are Skin Crave Spf30 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Skin Crave Spf30 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:
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)
- HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- PPG-15 STEARYL ETHER BENZOATE (UNII: 80D2J6361M)
- CUPRIC TRIETHANOLAMINE (UNII: 6NU949U74E)
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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".