NDC 12027-100 Wet N Wild Megashield
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12027 - Markwins Beauty Products, Inc
- 12027-100 - Wet N Wild
Product Packages
NDC Code 12027-100-10
Package Description: 3.1 g in 1 TUBE
Product Details
What is NDC 12027-100?
What are the uses for Wet N Wild Megashield?
Which are Wet N Wild Megashield UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Wet N Wild Megashield 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:
- CERESIN (UNII: Q1LS2UJO3A)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- TRIDECYL STEARATE (UNII: A8OE252M6L)
- PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- RICE GERM OIL (UNII: D4H5GGS5JF)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- COCHINEAL (UNII: TZ8Z31B35M)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- MICA (UNII: V8A1AW0880)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ZINC OXIDE (UNII: SOI2LOH54Z)
* 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".