NDC 0363-1117 Creal Zink Sunscreen Spf 50 Well At Walgreens
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreens
- 0363-1117 - Creal Zink Sunscreen Spf 50
Product Packages
NDC Code 0363-1117-01
Package Description: 14 g in 1 TUBE
Product Details
What is NDC 0363-1117?
Which are Creal Zink Sunscreen Spf 50 Well At Walgreens 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)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Creal Zink Sunscreen Spf 50 Well At Walgreens 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
* 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".