NDC 52731-7014 Cough Complex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52731 - Nova Homeopathic Therapeutics, Inc.
- 52731-7014 - Cough Complex
Product Packages
NDC Code 52731-7014-2
Package Description: 1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE (52731-7014-1)
Product Details
What is NDC 52731-7014?
What are the uses for Cough Complex?
Which are Cough Complex UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
- ANTIMONY (UNII: 9IT35J3UV3) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- PROTORTONIA CACTI (UNII: LZB7TFX1LT)
- PROTORTONIA CACTI (UNII: LZB7TFX1LT) (Active Moiety)
- CUPRIC ACETATE (UNII: 39M11XPH03)
- CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
- DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ)
- DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (Active Moiety)
- WOOD CREOSOTE (UNII: 3JYG22FD73)
- WOOD CREOSOTE (UNII: 3JYG22FD73) (Active Moiety)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- LOBARIA PULMONARIA (UNII: D1YM0P5Z2T)
- LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (Active Moiety)
Which are Cough Complex 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)
* 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".