NDC 70281-661 Goodsense Sunscreen Spf 70
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70281 - Solskyn Personal Care Llc
- 70281-661 - Goodsense Sunscreen Spf 70
Product Packages
NDC Code 70281-661-24
Package Description: 237 g in 1 CONTAINER
Product Details
What is NDC 70281-661?
What are the uses for Goodsense Sunscreen Spf 70?
Which are Goodsense Sunscreen Spf 70 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Goodsense Sunscreen Spf 70 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:
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- UNDECYLENIC ACID (UNII: K3D86KJ24N)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
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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".