NDC 63287-420 Shing-releev
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63287-420?
What are the uses for Shing-releev?
Which are Shing-releev UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZYL ALCOHOL (UNII: LKG8494WBH) (Active Moiety)
Which are Shing-releev 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)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ECHINACEA PURPUREA FLOWERING TOP (UNII: 2EMS3QFX65)
What is the NDC to RxNorm Crosswalk for Shing-releev?
- RxCUI: 1292894 - allantoin 0.5 % / benzalkonium chloride 0.13 % / benzyl alcohol 0.5 % Topical Spray
- RxCUI: 1292894 - allantoin 5 MG/ML / benzalkonium chloride 1.3 MG/ML / benzyl alcohol 0.005 ML/ML Topical Spray
- RxCUI: 1292897 - Shing-RELEEV 0.13 % / 0.5 % / 0.5 % Topical Spray
- RxCUI: 1292897 - allantoin 5 MG/ML / benzalkonium chloride 1.3 MG/ML / benzyl alcohol 0.005 ML/ML Topical Spray [Shing-Releev]
- RxCUI: 1292897 - Shing-Releev (allantoin 0.5 % / benzalkonium chloride 0.13 % / benzyl alcohol 0.5 % ) Topical Spray
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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".