NDC 63776-400 Ouch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63776 - Viatrexx Bio Incorporated
- 63776-400 - Ouch
Product Packages
NDC Code 63776-400-14
Package Description: 1 BOTTLE, SPRAY in 1 BOX / 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 63776-400?
What are the uses for Ouch?
Which are Ouch UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT (UNII: ML4QRZ1HCL)
- ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT (UNII: ML4QRZ1HCL) (Active Moiety)
- APOMORPHINE (UNII: N21FAR7B4S)
- APOMORPHINE (UNII: N21FAR7B4S) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- METENKEFALIN (UNII: 9JEZ9OD3AS)
- METENKEFALIN (UNII: 9JEZ9OD3AS) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7)
- BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7) (Active Moiety)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (Active Moiety)
- BOS TAURUS LIMBIC SYSTEM (UNII: 28WIH9KKYG)
- BOS TAURUS LIMBIC SYSTEM (UNII: 28WIH9KKYG) (Active Moiety)
- SUS SCROFA LIMBIC SYSTEM (UNII: F7PEN4AZI7)
- SUS SCROFA LIMBIC SYSTEM (UNII: F7PEN4AZI7) (Active Moiety)
- BOS TAURUS NERVE (UNII: 28G2U3MQJK)
- BOS TAURUS NERVE (UNII: 28G2U3MQJK) (Active Moiety)
- SUS SCROFA NERVE (UNII: JXV50I6ZHK)
- SUS SCROFA NERVE (UNII: JXV50I6ZHK) (Active Moiety)
- BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K)
- BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K) (Active Moiety)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (Active Moiety)
Which are Ouch 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)
- ALCOHOL (UNII: 3K9958V90M)
* 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".