NDC 37205-616 Ice External Analgesic Leader
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 37205 - Cardinal Health
- 37205-616 - Ice External Analgesic
Product Packages
NDC Code 37205-616-34
Package Description: 227 g in 1 JAR
Product Details
What is NDC 37205-616?
What are the uses for Ice External Analgesic Leader?
Which are Ice External Analgesic Leader UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Ice External Analgesic Leader 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:
- AMMONIA (UNII: 5138Q19F1X)
- CARBOMER 934 (UNII: Z135WT9208)
- CUPRIC SULFATE (UNII: LRX7AJ16DT)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- THYMOL (UNII: 3J50XA376E)
- WATER (UNII: 059QF0KO0R)
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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".