NDC 10755-030 Tourist Spf30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10755 - Island Company Lifestyle Products, Llc
- 10755-030 - Tourist Spf30
Product Packages
NDC Code 10755-030-02
Package Description: 60.9 g in 1 PACKAGE
NDC Code 10755-030-08
Package Description: 236 g in 1 BOTTLE
Product Details
What is NDC 10755-030?
What are the uses for Tourist Spf30?
Which are Tourist Spf30 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)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Tourist Spf30 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:
- ADIPIC ACID (UNII: 76A0JE0FKJ)
- DIETHYLENE GLYCOL (UNII: 61BR964293)
- GLYCERIN (UNII: PDC6A3C0OX)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- TROLAMINE (UNII: 9O3K93S3TK)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ALLANTOIN (UNII: 344S277G0Z)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
* 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".