NDC 0363-3191 Walgreens Cold Sore Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreens
- 0363-3191 - Walgreens Cold Sore Treatment
Product Characteristics
Product Packages
NDC Code 0363-3191-01
Package Description: 1 g in 1 CONTAINER
Product Details
What is NDC 0363-3191?
What are the uses for Walgreens Cold Sore Treatment?
Which are Walgreens Cold Sore Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Walgreens Cold Sore Treatment 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:
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- DOCOSANOL (UNII: 9G1OE216XY)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SUCROSE STEARATE (UNII: 274KW0O50M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- 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".