NDC 0573-0246 Anbesol Cold Sore Therapy
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0573 - Glaxosmithkline Consumer Healthcare Holdings (us) Llc
- 0573-0246 - Anbesol Cold Sore Therapy
Product Characteristics
Product Packages
NDC Code 0573-0246-26
Package Description: 1 TUBE in 1 BLISTER PACK / 9 g in 1 TUBE
Product Details
What is NDC 0573-0246?
What are the uses for Anbesol Cold Sore Therapy?
Which are Anbesol Cold Sore Therapy UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Anbesol Cold Sore Therapy 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOCETYL STEARATE (UNII: 3RJ7186O9W)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MINERAL OIL (UNII: T5L8T28FGP)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- WHITE WAX (UNII: 7G1J5DA97F)
What is the NDC to RxNorm Crosswalk for Anbesol Cold Sore Therapy?
- RxCUI: 1006096 - allantoin 1 % / benzocaine 20 % / camphor 3 % / petrolatum 64.9 % Topical Ointment
- RxCUI: 1006096 - allantoin 0.01 MG/MG / benzocaine 0.2 MG/MG / camphor 0.03 MG/MG / petrolatum 0.649 MG/MG Topical Ointment
- RxCUI: 1006096 - allantoin 1 % / benzocaine 20 % / camphor 3 % / petrolatum, white 64.9 % Topical Ointment
- RxCUI: 1052620 - Anbesol Cold Sore Therapy 1 % / 20 % / 3 % / 64.9 % Topical Ointment
- RxCUI: 1052620 - allantoin 0.01 MG/MG / benzocaine 0.2 MG/MG / camphor 0.03 MG/MG / petrolatum 0.649 MG/MG Topical Ointment [Anbesol Cold Sore Therapy]
* Please review the disclaimer below.
[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".