NDC 63354-998 Wet Ones
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 63354-998-14
Package Description: 144 SWAB in 1 PACKAGE
NDC Code 63354-998-20
Package Description: 20 SWAB in 1 POUCH
NDC Code 63354-998-24
Package Description: 24 SWAB in 1 PACKAGE
NDC Code 63354-998-28
Package Description: 28 SWAB in 1 POUCH
NDC Code 63354-998-40
Package Description: 40 SWAB in 1 CANISTER
NDC Code 63354-998-48
Package Description: 48 SWAB in 1 CANISTER
NDC Code 63354-998-65
Package Description: 65 SWAB in 1 CANISTER
Product Details
What is NDC 63354-998?
What are the uses for Wet Ones?
Which are Wet Ones UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Wet Ones 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:
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM CAPRYLOAMPHOPROPIONATE (UNII: W9H6IT16GQ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- PEG-60 LANOLIN (UNII: K2OI1D27ET)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALCOHOL (UNII: 3K9958V90M)
- QUATERNIUM-52 (UNII: 588EQF3H1P)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLPARABEN (UNII: 14255EXE39)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Wet Ones?
- RxCUI: 1043348 - benzethonium Cl 0.3 % Medicated Pad
- RxCUI: 1043348 - benzethonium chloride 3 MG/ML Medicated Pad
- RxCUI: 1043348 - benzethonium chloride 0.3 % Medicated Wipe
- RxCUI: 1043348 - benzethonium chloride 0.3 % Topical Cloth
* 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".