NDC 11822-3410 Rite Aid Renewal Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 11822-3410?
What are the uses for Rite Aid Renewal Sunscreen?
Which are Rite Aid Renewal Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Rite Aid Renewal 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- TROLAMINE (UNII: 9O3K93S3TK)
- BEHENYL PHOSPHATE (UNII: 366D9UAY69)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CODIUM TOMENTOSUM (UNII: B8B45BRU87)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- 1,2-BUTANEDIOL (UNII: RUN0H01QEU)
- TRIMETHYLOLPROPANE TRIETHYLHEXANOATE (UNII: B952ZGW1IL)
- CAPRYLIC/CAPRIC MONO/DIGLYCERIDES (UNII: U72Q2I8C85)
- ANISACRIL (UNII: 5TB1FV429Z)
- GUAR GUM (UNII: E89I1637KE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* 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".