NDC 50523-101 Spa Mystique Skin Protection Soothing Relief Moisturizing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50523 - Volume Distributors, Inc.
- 50523-101 - Spa Mystique Skin Protection Soothing Relief Moisturizing
Product Packages
NDC Code 50523-101-08
Package Description: 235 mL in 1 TUBE
Product Details
What is NDC 50523-101?
What are the uses for Spa Mystique Skin Protection Soothing Relief Moisturizing?
Which are Spa Mystique Skin Protection Soothing Relief Moisturizing UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Spa Mystique Skin Protection Soothing Relief Moisturizing 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:
- OAT (UNII: Z6J799EAJK)
- MINERAL OIL (UNII: T5L8T28FGP)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Spa Mystique Skin Protection Soothing Relief Moisturizing?
- RxCUI: 309916 - dimethicone 1.3 % Topical Cream
- RxCUI: 309916 - dimethicone 13 MG/ML Topical Cream
- RxCUI: 309916 - dimethicone 0.65 GM per 50 ML Topical Cream
- RxCUI: 309916 - dimethicone 1.95 GM per 150 ML 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".