NDC 79518-079 Dr. Du-mores Viral Defense Nano Gold Anti-aging Skin Disinfectant Protectant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79518 - Core Pacific, Inc.
- 79518-079 - Dr. Du-mores Viral Defense Nano Gold Anti-aging Skin Disinfectant Protectant
Product Packages
NDC Code 79518-079-01
Package Description: 59.14 mL in 1 BOTTLE, SPRAY
NDC Code 79518-079-02
Package Description: 237 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 79518-079?
What are the uses for Dr. Du-mores Viral Defense Nano Gold Anti-aging Skin Disinfectant Protectant?
Which are Dr. Du-mores Viral Defense Nano Gold Anti-aging Skin Disinfectant Protectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Dr. Du-mores Viral Defense Nano Gold Anti-aging Skin Disinfectant Protectant 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)
- SODIUM SESQUICARBONATE (UNII: Y1X815621J)
- MAGNESIUM (UNII: I38ZP9992A)
- SILVER (UNII: 3M4G523W1G)
- GOLD (UNII: 79Y1949PYO)
What is the NDC to RxNorm Crosswalk for Dr. Du-mores Viral Defense Nano Gold Anti-aging Skin Disinfectant Protectant?
- RxCUI: 1049254 - benzalkonium chloride 0.13 % Topical Solution
- RxCUI: 1049254 - benzalkonium chloride 1.3 MG/ML Topical Solution
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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".