NDC 70281-601 Goodsense Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70281 - Solskyn Personal Care Llc
- 70281-601 - Goodsense Sunscreen Spf 30
Product Packages
NDC Code 70281-601-24
Package Description: 237 g in 1 CONTAINER
Product Details
What is NDC 70281-601?
What are the uses for Goodsense Sunscreen Spf 30?
Which are Goodsense Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Goodsense Sunscreen Spf 30 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:
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- METHYL GLUCOSE (UNII: QCF122NF3R)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- EDETIC ACID (UNII: 9G34HU7RV0)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".