NDC 70233-010 Ultimate Skin Protectant Derma Shield
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70233-010?
What are the uses for Ultimate Skin Protectant Derma Shield?
Which are Ultimate Skin Protectant Derma Shield UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Ultimate Skin Protectant Derma Shield 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:
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ISOBUTANE (UNII: BXR49TP611)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- EDETIC ACID (UNII: 9G34HU7RV0)
- LANOLIN (UNII: 7EV65EAW6H)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- PALM KERNEL ACID (UNII: 79P21R4317)
- COPOVIDONE K25-31 (UNII: D9C330MD8B)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PALMITIC ACID (UNII: 2V16EO95H1)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PERFLUOROPOLYMETHYLISOPROPYL ETHER (UNII: X6324K3MBW)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPANE (UNII: T75W9911L6)
- BUTANE (UNII: 6LV4FOR43R)
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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".