NDC 77824-000 Dodys
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77824 - Betone, S.a. De C.v.
- 77824-000 - Dodys
Product Packages
NDC Code 77824-000-48
Package Description: 48 PATCH in 1 POUCH / 62.4 g in 1 PATCH
Product Details
What is NDC 77824-000?
What are the uses for Dodys?
Which are Dodys UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Dodys 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Dodys?
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM 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".