NDC 58132-3331 Alcis Daily Relief Pain Relief
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What is NDC 58132-3331?
What are the uses for Alcis Daily Relief Pain Relief?
Which are Alcis Daily Relief Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- TROLAMINE SALICYLATE (UNII: H8O4040BHD)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Alcis Daily Relief Pain Relief 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:
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CHAMOMILE (UNII: FGL3685T2X)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- IMIDUREA (UNII: M629807ATL)
- LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
- GLYCERYL DISTEARATE (UNII: 73071MW2KM)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- ROSEMARY (UNII: IJ67X351P9)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Alcis Daily Relief Pain Relief?
- RxCUI: 313518 - trolamine salicylate 10 % Topical Cream
- RxCUI: 313518 - trolamine salicylate 100 MG/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".