NDC 81119-001 Smile Antibacterial Wet Wipes Plantain Extract
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81119 - Kpd, Limited Liability Company
- 81119-001 - Smile Antibacterial Wet Wipes Plantain Extract
Product Packages
NDC Code 81119-001-15
Package Description: 15 PATCH in 1 PACKAGE / 2.28 mL in 1 PATCH
Product Details
What is NDC 81119-001?
What are the uses for Smile Antibacterial Wet Wipes Plantain Extract?
Which are Smile Antibacterial Wet Wipes Plantain Extract UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Smile Antibacterial Wet Wipes Plantain Extract 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PLANTAGO MAJOR LEAF (UNII: 7DC28K241X)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)
- ETHYLPARABEN (UNII: 14255EXE39)
- BRONOPOL (UNII: 6PU1E16C9W)
- CETRIMONIUM BROMIDE (UNII: L64N7M9BWR)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- CITRAL (UNII: T7EU0O9VPP)
What is the NDC to RxNorm Crosswalk for Smile Antibacterial Wet Wipes Plantain Extract?
- 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
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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".