NDC 70381-122 Daily Defense Colloidal Oatmeal For Face And Eyes
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70381-122?
What are the uses for Daily Defense Colloidal Oatmeal For Face And Eyes?
Which are Daily Defense Colloidal Oatmeal For Face And Eyes UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are Daily Defense Colloidal Oatmeal For Face And Eyes 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)
- SHEA BUTTER (UNII: K49155WL9Y)
- PROPANEDIOL (UNII: 5965N8W85T)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- OAT (UNII: Z6J799EAJK)
- BETAINE (UNII: 3SCV180C9W)
- OPHIOPOGON JAPONICUS ROOT (UNII: 90PS6JV9GZ)
- NIACINAMIDE (UNII: 25X51I8RD4)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- LAURYL LAURATE (UNII: GPW77G0937)
- CETYL MYRISTATE (UNII: 7OPL833Q4D)
- HECTORITE (UNII: 08X4KI73EZ)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- SODIUM POLYACRYLATE STARCH (25 MICROMETER PARTICLE) (UNII: KXY4EH7RJV)
What is the NDC to RxNorm Crosswalk for Daily Defense Colloidal Oatmeal For Face And Eyes?
- RxCUI: 240651 - colloidal oatmeal 1 % Topical Cream
- RxCUI: 240651 - colloidal oatmeal 10 MG/ML Topical Cream
- RxCUI: 240651 - Avena sativa 1 % Topical Cream
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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".