NDC 69837-500 Sure Result Dss Premium Pak
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 69837-500?
Which are Sure Result Dss Premium Pak UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOFENAC SODIUM (UNII: QTG126297Q)
- DICLOFENAC (UNII: 144O8QL0L1) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
Which are Sure Result Dss Premium Pak 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:
- DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA (UNII: O80TY208ZW)
- BOSWELLIA SERRATA RESIN OIL (UNII: 5T1XCE6K8K)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYETHYLENE GLYCOL 800 (UNII: UH6KR4953D)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- TRIETHANOLAMINE GLUTAMATE (UNII: M71CZB7HUY)
What is the NDC to RxNorm Crosswalk for Sure Result Dss Premium Pak?
- RxCUI: 857700 - diclofenac sodium 1.5 % Topical Solution
- RxCUI: 857700 - diclofenac sodium 15 MG/ML Topical Solution
- RxCUI: 857700 - diclofenac sodium 1.5 % (as diclofenac sodium 16.05 MG/ML) Topical Solution
- RxCUI: 857700 - diclofenac sodium 16.05 MG per 1 ML Topical Solution
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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".