NDC 69475-5411 Derma Breeze Skin Protectant Cream
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What is NDC 69475-5411?
What are the uses for Derma Breeze Skin Protectant Cream?
Which are Derma Breeze Skin Protectant Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are Derma Breeze Skin Protectant Cream 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:
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CURDLAN (UNII: 6930DL209R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ISOCETYL STEARATE (UNII: 3RJ7186O9W)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- LACTIC ACID (UNII: 33X04XA5AT)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PPG-51/SMDI COPOLYMER (UNII: KQ9JG3O3YA)
- WATER (UNII: 059QF0KO0R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL STEARATE (UNII: MZM1I680W0)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PEG-10 SOY STEROL (UNII: FG54K98L0Q)
What is the NDC to RxNorm Crosswalk for Derma Breeze Skin Protectant Cream?
- 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".