NDC 69299-201 Dr. Throwers Beta
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69299 - Dr. Thrower's Skincare, Inc.
- 69299-201 - Dr. Throwers Beta
Product Packages
NDC Code 69299-201-22
Package Description: 56 g in 1 JAR
Product Details
What is NDC 69299-201?
What are the uses for Dr. Throwers Beta?
Which are Dr. Throwers Beta UNII Codes?
The UNII codes for the active ingredients in this product are:
- BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U)
- BETAMETHASONE (UNII: 9842X06Q6M) (Active Moiety)
Which are Dr. Throwers Beta 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)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALCOHOL (UNII: 3K9958V90M)
- DECYL OLEATE (UNII: ZGR06DO97T)
- HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP)
- HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C)
- HYDROGENATED COTTONSEED OIL (UNII: Z82Y2C65EA)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Dr. Throwers Beta?
- RxCUI: 238920 - betamethasone 0.05 % Topical Cream
- RxCUI: 238920 - betamethasone 0.5 MG/ML Topical Cream
- RxCUI: 238920 - betamethasone 0.5 MG/GM (betamethasone dipropionate 0.64 MG/GM) Topical Cream
* 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".