NDC 73923-0120 Innerest Mediwiper
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73923 - Firstcham Co., Ltd
- 73923-0120 - Innerest Mediwiper
Product Packages
NDC Code 73923-0120-1
Package Description: 54 g in 1 CONTAINER
NDC Code 73923-0120-2
Package Description: 108 g in 1 CONTAINER
NDC Code 73923-0120-3
Package Description: 432 g in 1 CONTAINER
Product Details
What is NDC 73923-0120?
What are the uses for Innerest Mediwiper?
Which are Innerest Mediwiper UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Innerest Mediwiper 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:
- WATER (UNII: 059QF0KO0R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Innerest Mediwiper?
- RxCUI: 1038856 - benzalkonium Cl 0.1 % Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 1 MG/ML Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 0.1 % Medicated Wipes
- RxCUI: 1038856 - benzalkonium chloride 0.1 % Topical Swab
* 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".