NDC 69666-368 Blue Ice Pain Relieving
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69666 - Genuine Drugs
- 69666-368 - Blue Ice
Product Characteristics
Product Packages
NDC Code 69666-368-08
Package Description: 1 JAR in 1 BOX / 227 g in 1 JAR
Product Details
What is NDC 69666-368?
What are the uses for Blue Ice Pain Relieving?
Which are Blue Ice Pain Relieving UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
Which are Blue Ice Pain Relieving 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)
- 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)
What is the NDC to RxNorm Crosswalk for Blue Ice Pain Relieving?
- RxCUI: 1606045 - capsaicin 0.025 % / menthol 5 % Topical Gel
- RxCUI: 1606045 - capsaicin 0.00025 MG/MG / menthol 0.05 MG/MG Topical Gel
* 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".