NDC 60512-2005 Cough And Cold Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60512 - Homeolab Usa Inc.
- 60512-2005 - Cough And Cold Relief
Product Packages
NDC Code 60512-2005-4
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 60512-2005?
What are the uses for Cough And Cold Relief?
Which are Cough And Cold Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ)
- DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- IPECAC (UNII: 62I3C8233L)
- IPECAC (UNII: 62I3C8233L) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- ATROPA BELLADONNA WHOLE (UNII: DSV74G1P2J)
- ATROPA BELLADONNA WHOLE (UNII: DSV74G1P2J) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
Which are Cough And Cold Relief 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".