NDC 62382-0322 Easy To Break-off Cleaning And Disinfecting Swabstick Dfb-i
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62382 - Longood Medicine (beijing) Co., Ltd.
- 62382-0322 - Easy To Break-off Cleaning And Disinfecting Swabstick Dfb-i
Product Packages
NDC Code 62382-0322-1
Package Description: .2 mL in 1 POUCH
NDC Code 62382-0322-2
Package Description: .3 mL in 1 POUCH
NDC Code 62382-0322-3
Package Description: .4 mL in 1 POUCH
NDC Code 62382-0322-4
Package Description: .5 mL in 1 POUCH
NDC Code 62382-0322-5
Package Description: .6 mL in 1 POUCH
Product Details
What is NDC 62382-0322?
What are the uses for Easy To Break-off Cleaning And Disinfecting Swabstick Dfb-i?
Which are Easy To Break-off Cleaning And Disinfecting Swabstick Dfb-i UNII Codes?
The UNII codes for the active ingredients in this product are:
- POVIDONE-IODINE (UNII: 85H0HZU99M)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
Which are Easy To Break-off Cleaning And Disinfecting Swabstick Dfb-i 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)
- NONOXYNOL-10 (UNII: K7O76887AP)
What is the NDC to RxNorm Crosswalk for Easy To Break-off Cleaning And Disinfecting Swabstick Dfb-i?
- RxCUI: 1037205 - povidone-iodine 1 % Medicated Pad
- RxCUI: 1037205 - povidone-iodine 10 MG/ML Medicated Pad
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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".