NDC 58892-070 Cotz Plus Spf 58 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 58892-070?
What are the uses for Cotz Plus Spf 58 Sunscreen?
Which are Cotz Plus Spf 58 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Cotz Plus Spf 58 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- ISOPROPYLPARABEN (UNII: A6EOX47QK0)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- TALC (UNII: 7SEV7J4R1U)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRICONTANYL POVIDONE (4 TRICONTANYL BRANCHES/REPEAT) (UNII: N0SS3Q238D)
- WATER (UNII: 059QF0KO0R)
- 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".