NDC 12027-102 Wet N Wild Ultimate Match
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12027 - Markwins Beauty Products, Inc
- 12027-102 - Wet N Wild
Product Packages
NDC Code 12027-102-29
Package Description: 29.6 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 12027-102?
What are the uses for Wet N Wild Ultimate Match?
Which are Wet N Wild Ultimate Match 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 Ultimate Match 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)
- TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
- TALC (UNII: 7SEV7J4R1U)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ISODODECANE (UNII: A8289P68Y2)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- TRIACONTANYL PVP (WP-660) (UNII: N0SS3Q238D)
- TROLAMINE (UNII: 9O3K93S3TK)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- DISODIUM GLYCYRRHIZATE (UNII: L8Q0US0J7V)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
- LAMINARIA OCHROLEUCA (UNII: 4R2124HE76)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
* 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".