NDC 58892-318 Solar Protection Formula Tizo Spf 35 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 58892-318?
What are the uses for Solar Protection Formula Tizo Spf 35 Sunscreen?
Which are Solar Protection Formula Tizo Spf 35 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Solar Protection Formula Tizo Spf 35 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:
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE 100 (UNII: RO266O364U)
- DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- STEARYL DIMETHICONE (400 MPA.S AT 50C) (UNII: R327X197HY)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Solar Protection Formula Tizo Spf 35 Sunscreen?
- RxCUI: 244637 - zinc oxide 20 % Topical Lotion
- RxCUI: 244637 - zinc oxide 200 MG/ML Topical Lotion
- RxCUI: 244637 - ZnO 20 % Topical Lotion
- RxCUI: 244637 - ZNO 200 MG/ML Topical Lotion
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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".