NDC 69711-360 Chorus Supernatural Protect Spf 30 Broad Spectrum Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 69711-360?
What are the uses for Chorus Supernatural Protect Spf 30 Broad Spectrum Sunscreen?
Which are Chorus Supernatural Protect Spf 30 Broad Spectrum Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Chorus Supernatural Protect Spf 30 Broad Spectrum Sunscreen 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:
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- GLYCERIN (UNII: PDC6A3C0OX)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- WATER (UNII: 059QF0KO0R)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PANTHENOL (UNII: WV9CM0O67Z)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- TOCOPHEROL (UNII: R0ZB2556P8)
- FYTIC ACID (UNII: 7IGF0S7R8I)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CARBOXYMETHYLCELLULOSE CALCIUM (UNII: UTY7PDF93L)
- XANTHAN GUM (UNII: TTV12P4NEE)
* 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".