NDC 64058-154 Charley Horse
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64058 - Concept Laboratories, Inc.
- 64058-154 - Charley Horse
Product Packages
NDC Code 64058-154-34
Package Description: 113 g in 1 JAR
Product Details
What is NDC 64058-154?
What are the uses for Charley Horse?
Which are Charley Horse UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- CUPRIC ARSENITE (UNII: SK8L60BCSQ)
- CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
- ARSENITE ION (UNII: N5509X556J) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
Which are Charley Horse 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:
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM ACRYLATE (UNII: 7C98FKB43H)
- WATER (UNII: 059QF0KO0R)
* 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".