NDC 58686-013 Shunfa Anti-bacteria Spra
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 58686-013?
What are the uses for Shunfa Anti-bacteria Spra?
Which are Shunfa Anti-bacteria Spra UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIDECYLDIMETHYLAMMONIUM (UNII: Z7F472XQPA)
- DIDECYLDIMETHYLAMMONIUM (UNII: Z7F472XQPA) (Active Moiety)
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
- BENZALKONIUM BROMIDE (UNII: 151T1GQ42D)
- BENZALKONIUM BROMIDE (UNII: 151T1GQ42D) (Active Moiety)
- BORNEOL (UNII: M89NIB437X)
- BORNEOL (UNII: M89NIB437X) (Active Moiety)
Which are Shunfa Anti-bacteria Spra 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:
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- MENTHOL (UNII: L7T10EIP3A)
- WATER (UNII: 059QF0KO0R)
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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".