NDC 66428-002 Theradermspf 43 Spf 43
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 66428-002?
What are the uses for Theradermspf 43 Spf 43?
Which are Theradermspf 43 Spf 43 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Theradermspf 43 Spf 43 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)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- OCTYL STEARATE (UNII: 772Y4UFC8B)
- ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERETH-26 (UNII: NNE56F2N14)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PANTHENOL (UNII: WV9CM0O67Z)
- ALLANTOIN (UNII: 344S277G0Z)
- OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)
- 2-HYDROXYETHYL ACRYLATE (UNII: 25GT92NY0C)
- POLYISOBUTYLENE (1300 MW) (UNII: 241BN7J12Y)
- COCONUT ALCOHOL (UNII: 13F4MW8Y9K)
- POLYESTER-7 (UNII: 0841698D2F)
- ETHYLENE OXIDE (UNII: JJH7GNN18P)
- POLYETHYLENE GLYCOL 350 (UNII: ZBR3T82M2V)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
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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".