NDC 63354-998 Wet Ones

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
Proprietary Name:
Wet Ones
Product Type: [3]
Labeler Name: [5]
Edgewell Personal Care Brands Llc
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Navigator:

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?

The NDC code 63354-998 is assigned by the FDA to the product Wet Ones which is product labeled by Edgewell Personal Care Brands Llc. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 63354-998-14 144 swab in 1 package , 63354-998-20 20 swab in 1 pouch , 63354-998-24 24 swab in 1 package , 63354-998-28 28 swab in 1 pouch , 63354-998-40 40 swab in 1 canister , 63354-998-48 48 swab in 1 canister , 63354-998-65 65 swab in 1 canister . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Wet Ones?

Adults and children 2 years and overapply to handsallow skin to dry without wipingchildren under 2 yearsask a doctor before use

Which are Wet Ones UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Wet Ones?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[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".