NDC 70458-103 Dyve Comfort L
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70458 - Ampersand Biopharmaceuticals
- 70458-103 - Dyve Comfort L
Product Packages
NDC Code 70458-103-20
Package Description: 1 JAR in 1 BOX / 200 g in 1 JAR
Product Details
What is NDC 70458-103?
What are the uses for Dyve Comfort L?
Which are Dyve Comfort L UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Dyve Comfort L 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:
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- WATER (UNII: 059QF0KO0R)
- POLYGLYCERYL-4 STEARATE (UNII: VLC3W3U1PE)
- PALM KERNEL OIL (UNII: B0S90M0233)
- POLYGLYCERYL-4 OLEATE (UNII: 15B05TY4GX)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Dyve Comfort L?
- RxCUI: 1804176 - lidocaine 4 % / menthol 1 % Topical Gel
- RxCUI: 1804176 - lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Topical Gel
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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".