NDC 63083-4003 Virus Nosode 4003
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-4003 - Virus Nosode
Product Packages
NDC Code 63083-4003-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-4003?
What are the uses for Virus Nosode 4003?
Which are Virus Nosode 4003 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BACILLUS CALMETTE-GUERIN LIVE ANTIGEN, UNSPECIFIED SUBSTRAIN (UNII: 8VJE55B0VG)
- BACILLUS CALMETTE-GUERIN LIVE ANTIGEN, UNSPECIFIED SUBSTRAIN (UNII: 8VJE55B0VG) (Active Moiety)
- COXSACKIEVIRUS A21 (UNII: 4B57CWT710)
- COXSACKIEVIRUS A21 (UNII: 4B57CWT710) (Active Moiety)
- HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K)
- HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K) (Active Moiety)
- HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX)
- HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX) (Active Moiety)
- HAEMOPHILUS INFLUENZAE (UNII: K738E2MB3I)
- HAEMOPHILUS INFLUENZAE (UNII: K738E2MB3I) (Active Moiety)
- POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 0LVY784C09)
- POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 0LVY784C09) (Active Moiety)
- DALEA FOLIOLOSA WHOLE (UNII: R2ZFR12IQ9)
- DALEA FOLIOLOSA WHOLE (UNII: R2ZFR12IQ9) (Active Moiety)
- DRABA VERNA WHOLE (UNII: 11I0GD34ZJ)
- DRABA VERNA WHOLE (UNII: 11I0GD34ZJ) (Active Moiety)
- VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK)
- VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK) (Active Moiety)
- HUMAN VARICELLA-ZOSTER IMMUNE GLOBULIN (UNII: 33T61IWL27)
- HUMAN VARICELLA-ZOSTER IMMUNE GLOBULIN (UNII: 33T61IWL27) (Active Moiety)
Which are Virus Nosode 4003 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:
- ALCOHOL (UNII: 3K9958V90M)
- 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".