NDC 72933-006 Arumacil Protectant Cold Sore
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72933 - Hyatt Life Sciences, Inc.
- 72933-006 - Arumacil Protectant Cold Sore
Product Packages
NDC Code 72933-006-01
Package Description: 1 TUBE in 1 BLISTER PACK / 7.5 g in 1 TUBE
Product Details
What is NDC 72933-006?
What are the uses for Arumacil Protectant Cold Sore?
Which are Arumacil Protectant Cold Sore UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Arumacil Protectant Cold Sore 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:
- ARUM PALAESTINUM WHOLE (UNII: 4E96UIB20M)
- .BETA.-SITOSTEROL (UNII: S347WMO6M4)
- TURMERIC (UNII: 856YO1Z64F)
- VANILLIN (UNII: CHI530446X)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
What is the NDC to RxNorm Crosswalk for Arumacil Protectant Cold Sore?
- RxCUI: 2122984 - dimethicone 1.1 % / petrolatum 92.8 % Topical Ointment
- RxCUI: 2122984 - dimethicone 0.011 MG/MG / petrolatum 0.928 MG/MG Topical Ointment
- RxCUI: 2122989 - Arumacil 1.1 % / 92.8 % Topical Ointment
- RxCUI: 2122989 - dimethicone 0.011 MG/MG / petrolatum 0.928 MG/MG Topical Ointment [Arumacil]
- RxCUI: 2122989 - Arumacil (dimethicone 1.1 % / petrolatum 92.8 % ) Topical Ointment
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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".