NDC 63354-998 Wet Ones

  1. Labeler Index
  2. Edgewell Personal Care Brands Llc
  3. NDC: 63354-998 Wet Ones

NDC Product Code 63354-998

NDC CODE: 63354-998

Proprietary Name: Wet Ones What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This product is used as antibacterial

NDC Code Structure

NDC 63354-998-14

Package Description: 144 SWAB in 1 PACKAGE

NDC 63354-998-20

Package Description: 20 SWAB in 1 POUCH

NDC 63354-998-24

Package Description: 24 SWAB in 1 PACKAGE

NDC 63354-998-28

Package Description: 28 SWAB in 1 POUCH

NDC 63354-998-40

Package Description: 40 SWAB in 1 CANISTER

NDC 63354-998-48

Package Description: 48 SWAB in 1 CANISTER

NDC 63354-998-65

Package Description: 65 SWAB in 1 CANISTER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Wet Ones with NDC 63354-998 is product labeled by Edgewell Personal Care Brands Llc. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.
  • 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)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Edgewell Personal Care Brands Llc
Labeler Code: 63354
Start Marketing Date: 10-01-2007 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2021 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.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Wet Ones Product Label Images

Wet Ones Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Benzethonium Chloride 0.3%

Purpose

Antibacterial

Use

Decrease bacteria on skin

Warnings

For external use only

Do Not Use

If you are allergic to any of the ingredients

When Using This Product

Do not get into eyes. If contact occurs, rinse thoroughly with water

Stop Use And Ask A Doctor

If irritation or rash develops and continues for more than 72 hours

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

Inactive Ingredients

Water, Alcohol Denat., PEG-8 Dimethicone, Phenoxyethanol, Quaternium-52, Potassium Sorbate, Sodium Capryloamphopropionate, Methylparaben, Citric Acid, Disodium EDTA, Fragrance, Ethylparaben, PEG-60 Lanolin, Propylparaben, Aloe Barbadensis Leaf Juice

Pdp

FRESHSCENTWetOnesANTIBACTERIALHAND WIPESKills 99.99% of Germscleans better thanhand sanitizershypoallergenic

* Please review the disclaimer below.