NDC 72941-932 Labisan Cold Sore
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72941 - Lupuca Pharma Gmbh
- 72941-932 - Labisan Cold Sore
Product Characteristics
Product Packages
NDC Code 72941-932-72
Package Description: 6.7 g in 1 TUBE
Product Details
What is NDC 72941-932?
What are the uses for Labisan Cold Sore?
Which are Labisan Cold Sore UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENOL (UNII: 339NCG44TV)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Labisan 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:
- OLIVE OIL (UNII: 6UYK2W1W1E)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- CASTOR OIL (UNII: D5340Y2I9G)
- TALC (UNII: 7SEV7J4R1U)
- PETROLATUM (UNII: 4T6H12BN9U)
- MINERAL OIL (UNII: T5L8T28FGP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Labisan Cold Sore?
- RxCUI: 2119083 - phenol 1.4 % / zinc oxide 20 % Topical Ointment
- RxCUI: 2119083 - phenol 0.014 MG/MG / zinc oxide 0.2 MG/MG Topical Ointment
- RxCUI: 2119083 - Phenol 0.014 MG/MG / ZNO 0.2 MG/MG 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".