NDC 52629-800 Assured
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52629 - Higiene + Salud, S.a. De C.v.
- 52629-800 - Assured
Product Packages
NDC Code 52629-800-03
Package Description: 16 PACKAGE in 1 BOX / 1 POUCH in 1 PACKAGE / .3 mg in 1 POUCH
Product Details
What is NDC 52629-800?
What are the uses for Assured?
Which are Assured UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Assured 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Assured?
- RxCUI: 2276303 - benzalkonium Cl 0.125 % Medicated Pad
- RxCUI: 2276303 - benzalkonium chloride 1.25 MG/ML Medicated Pad
- RxCUI: 2276303 - benzalkonium chloride 0.125 % Medicated Wipe
- RxCUI: 2276303 - benzalkonium chloride 0.125 % Topical Cloth
- RxCUI: 2276303 - benzalkonium chloride 0.125 % 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".