NDC 31774-8005 Labella Linimento Obrero
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 31774 - Golden Sun Inc Dba Newhall Laboratories
- 31774-8005 - Labella Linimento Obrero
Product Packages
NDC Code 31774-8005-1
Package Description: 236 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 31774-8005?
What are the uses for Labella Linimento Obrero?
Which are Labella Linimento Obrero UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Labella Linimento Obrero 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)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- EDETATE SODIUM (UNII: MP1J8420LU)
What is the NDC to RxNorm Crosswalk for Labella Linimento Obrero?
- RxCUI: 1721014 - capsaicin 0.025 % / menthol 2 % / methyl salicylate 10 % Topical Cream
- RxCUI: 1721014 - capsaicin 0.25 MG/ML / menthol 20 MG/ML / methyl salicylate 100 MG/ML 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".