NDC 69435-1905 Xxl Sun Block Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69435 - Peer Pharma Ltd.
- 69435-1905 - Xxl Sun Block Spf 50
Product Packages
NDC Code 69435-1905-1
Package Description: 100 mL in 1 CONTAINER
Product Details
What is NDC 69435-1905?
What are the uses for Xxl Sun Block Spf 50?
Which are Xxl Sun Block Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Xxl Sun Block Spf 50 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:
- JOJOBA OIL (UNII: 724GKU717M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ALMOND OIL (UNII: 66YXD4DKO9)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- ALLANTOIN (UNII: 344S277G0Z)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)
- SHEA BUTTER (UNII: K49155WL9Y)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- NIACINAMIDE (UNII: 25X51I8RD4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SEA SALT (UNII: 87GE52P74G)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PANTHENOL (UNII: WV9CM0O67Z)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- WATER (UNII: 059QF0KO0R)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
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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".