NDC 10210-0012 Carmex Cold Sore Treatment External Analgesic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10210 - Carma Laboratories, Inc.
- 10210-0012 - Carmex Cold Sore Treatment External Analgesic
Product Packages
NDC Code 10210-0012-0
Package Description: 2 g in 1 TUBE
Product Details
What is NDC 10210-0012?
What are the uses for Carmex Cold Sore Treatment External Analgesic?
Which are Carmex Cold Sore Treatment External Analgesic UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Carmex Cold Sore Treatment External Analgesic 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:
- CYCLOMETHICONE (UNII: NMQ347994Z)
- POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PETROLATUM (UNII: 4T6H12BN9U)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MENTHOL (UNII: L7T10EIP3A)
- STANNIC OXIDE (UNII: KM7N50LOS6)
What is the NDC to RxNorm Crosswalk for Carmex Cold Sore Treatment External Analgesic?
- RxCUI: 244550 - benzocaine 10 % Topical Cream
- RxCUI: 244550 - benzocaine 100 MG/ML Topical Cream
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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".