NDC 69642-1600 Antiphlamine Coin Plaster
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69642 - Hanul Trading Co., Ltd.
- 69642-1600 - Antiphlamine
Product Packages
NDC Code 69642-1600-2
Package Description: 84 PATCH in 1 CARTON / .2832 g in 1 PATCH (69642-1600-1)
Product Details
What is NDC 69642-1600?
What are the uses for Antiphlamine Coin Plaster?
Which are Antiphlamine Coin Plaster UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- LEVOMENTHOL (UNII: BZ1R15MTK7) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
- .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
- .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- PEPPERMINT (UNII: V95R5KMY2B) (Active Moiety)
- NONIVAMIDE (UNII: S846B891OR)
- NONIVAMIDE (UNII: S846B891OR) (Active Moiety)
Which are Antiphlamine Coin Plaster 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:
- MINERAL OIL (UNII: T5L8T28FGP)
* 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".