NDC 66134-042 Safe Sea Spf 40
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66134 - Sasa Cosmetics
- 66134-042 - Safe Sea Spf 40
Product Packages
NDC Code 66134-042-42
Package Description: 118 g in 1 BOTTLE, SPRAY
Product Details
What is NDC 66134-042?
What are the uses for Safe Sea Spf 40?
Which are Safe Sea Spf 40 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (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)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Safe Sea Spf 40 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
- CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- LANTHANUM CHLORIDE (UNII: 04M8624OXV)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
- PHAEODACTYLUM TRICORNUTUM (UNII: Y5W63E7HLV)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- POLYSULFATED GLYCOSAMINOGLYCAN (UNII: 268AW7000T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- TRIMETHOXYCAPRYLYLSILANE (UNII: FZ07E4LW2M)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
* 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".