NDC 71521-024 Diabetic Itch Relief Cream Professional
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71521 - Lavior Inc
- 71521-024 - Diabetic Itch Relief Cream Professional
Product Packages
NDC Code 71521-024-50
Package Description: 50 g in 1 BOTTLE, PUMP
Product Details
What is NDC 71521-024?
What are the uses for Diabetic Itch Relief Cream Professional?
Which are Diabetic Itch Relief Cream Professional UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are Diabetic Itch Relief Cream Professional 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- PROPANEDIOL (UNII: 5965N8W85T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- DITTRICHIA VISCOSA WHOLE (UNII: 3SYW69FH88)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- XANTHAN GUM (UNII: TTV12P4NEE)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
What is the NDC to RxNorm Crosswalk for Diabetic Itch Relief Cream Professional?
- 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".