NDC 47219-102 Cobroxin For Chronic Pain
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 47219 - Receptopharm Inc
- 47219-102 - Cobroxin
Product Packages
NDC Code 47219-102-52
Package Description: 1 BOTTLE, SPRAY in 1 BOX / 29 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 47219-102?
What are the uses for Cobroxin For Chronic Pain?
Which are Cobroxin For Chronic Pain UNII Codes?
The UNII codes for the active ingredients in this product are:
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM)
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (Active Moiety)
Which are Cobroxin For Chronic Pain 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ANHYDROUS TRISODIUM CITRATE (UNII: RS7A450LGA)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- XYLITOL (UNII: VCQ006KQ1E)
- 2-(DIETHYLAMINO)ETHANOL (UNII: S6DL4M053U)
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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".