NDC 69821-001 Antibacterial Wet Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69821 - Zhejiang Qimei Commodity Co.,ltd.
- 69821-001 - Antibacterial Wet Wipes
- 69821-001-01
- 69821-001-02
- 69821-001-03
- 69821-001-04
- 69821-001-05
- 69821-001-06
- 69821-001-07
- 69821-001-08
- 69821-001-09
- 69821-001-10
- 69821-001-11
- 69821-001-12
- 69821-001-13
- 69821-001-14
- 69821-001-15
- 69821-001-16
- 69821-001-17
- 69821-001-18
- 69821-001-19
- 69821-001-20
- 69821-001-21
- 69821-001-22
- 69821-001-23
- 69821-001-24
- 69821-001-25
- 69821-001-26
- 69821-001-27
- 69821-001 - Antibacterial Wet Wipes
Product Packages
NDC Code 69821-001-01
Package Description: 10 POUCH in 1 PACKAGE / .0042 g in 1 POUCH
NDC Code 69821-001-02
Package Description: 15 POUCH in 1 PACKAGE / .0042 g in 1 POUCH
NDC Code 69821-001-03
Package Description: 30 POUCH in 1 PACKAGE / .0042 g in 1 POUCH
NDC Code 69821-001-04
Package Description: 50 POUCH in 1 PACKAGE / .0042 g in 1 POUCH
NDC Code 69821-001-05
Package Description: 80 POUCH in 1 PACKAGE / .0042 g in 1 POUCH
NDC Code 69821-001-06
Package Description: 100 POUCH in 1 PACKAGE / .0042 g in 1 POUCH
NDC Code 69821-001-07
Package Description: 30 POUCH in 1 BOTTLE / .0042 g in 1 POUCH
NDC Code 69821-001-08
Package Description: 50 POUCH in 1 BOTTLE / .0042 g in 1 POUCH
NDC Code 69821-001-09
Package Description: 80 POUCH in 1 BOTTLE / .0042 g in 1 POUCH
NDC Code 69821-001-10
Package Description: 100 POUCH in 1 BOTTLE / .0042 g in 1 POUCH
NDC Code 69821-001-11
Package Description: 1 POUCH in 1 BAG / .0042 g in 1 POUCH
NDC Code 69821-001-12
Package Description: 250 POUCH in 1 CANISTER / .0042 g in 1 POUCH
NDC Code 69821-001-13
Package Description: 800 POUCH in 1 BAG / .0042 g in 1 POUCH
NDC Code 69821-001-14
Package Description: 1000 POUCH in 1 BAG / .0042 g in 1 POUCH
NDC Code 69821-001-15
Package Description: 1200 POUCH in 1 BAG / .0042 g in 1 POUCH
NDC Code 69821-001-16
Package Description: 1500 POUCH in 1 BAG / .0042 g in 1 POUCH
NDC Code 69821-001-17
Package Description: 16 POUCH in 1 BAG / .0042 g in 1 POUCH
NDC Code 69821-001-18
Package Description: 8 POUCH in 1 BAG / .36 g in 1 POUCH
NDC Code 69821-001-19
Package Description: 5 POUCH in 1 BAG / 225 g in 1 POUCH
NDC Code 69821-001-20
Package Description: 20 POUCH in 1 BAG / .9 g in 1 POUCH
NDC Code 69821-001-21
Package Description: 2000 POUCH in 1 BAG / 5.096 g in 1 POUCH
NDC Code 69821-001-22
Package Description: 1600 POUCH in 1 BAG / 4.077 g in 1 POUCH
NDC Code 69821-001-23
Package Description: 1800 POUCH in 1 BAG / 4.587 g in 1 POUCH
NDC Code 69821-001-24
Package Description: 2500 POUCH in 1 BAG / 6.37 g in 1 POUCH
NDC Code 69821-001-25
Package Description: 60 POUCH in 1 BAG / 6.37 g in 1 POUCH
NDC Code 69821-001-26
Package Description: 120 POUCH in 1 BAG / 6.37 g in 1 POUCH
NDC Code 69821-001-27
Package Description: 150 POUCH in 1 PAIL / 6.37 g in 1 POUCH
Product Details
What is NDC 69821-001?
What are the uses for Antibacterial Wet Wipes?
Which are Antibacterial Wet Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Antibacterial Wet Wipes 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
What is the NDC to RxNorm Crosswalk for Antibacterial Wet Wipes?
- 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".