51414-400 NDC - ANTIBACTERIAL WET WIPES (BENZALKONIUM CHLORIDE)

Drug Information

Product NDC: 51414-400

Proprietary Name: antibacterial wet wipes

Non Proprietary Name: Benzalkonium Chloride

Active Ingredient(s):
  • .13 g/100g BENZALKONIUM CHLORIDE


Administration Route(s): TOPICAL

Dosage Form(s): SWAB

Labeler Information

Labeler Name: Yuyao Jessie Commodity Co.,Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:5/8/2012

Package Information

No. Package Code Package Description Billing Unit
151414-400-011 POUCH in 1 BOTTLE (51414-400-01) / 10 g in 1 POUCH
251414-400-025 POUCH in 1 BOTTLE (51414-400-02) / 4 g in 1 POUCH
351414-400-0310 POUCH in 1 BOTTLE (51414-400-03) / 3.5 g in 1 POUCH
451414-400-0415 POUCH in 1 BOTTLE (51414-400-04) / 3 g in 1 POUCH
551414-400-0520 POUCH in 1 BOTTLE (51414-400-05) / 3 g in 1 POUCH
651414-400-0625 POUCH in 1 BOTTLE (51414-400-06) / 3 g in 1 POUCH
751414-400-0730 POUCH in 1 BOTTLE (51414-400-07) / 2.5 g in 1 POUCH
851414-400-0835 POUCH in 1 BOTTLE (51414-400-08) / 2.5 g in 1 POUCH
951414-400-0940 POUCH in 1 BOTTLE (51414-400-09) / 2.5 g in 1 POUCH
1051414-400-1045 POUCH in 1 BOTTLE (51414-400-10) / 2.5 g in 1 POUCH
1151414-400-1150 POUCH in 1 BOTTLE (51414-400-11) / 2.5 g in 1 POUCH
1251414-400-1260 POUCH in 1 BOTTLE (51414-400-12) / 2.5 g in 1 POUCH
1351414-400-1370 POUCH in 1 BOTTLE (51414-400-13) / 2.5 g in 1 POUCH
1451414-400-1480 POUCH in 1 BOTTLE (51414-400-14) / 2.5 g in 1 POUCH
1551414-400-1590 POUCH in 1 BOTTLE (51414-400-15) / 2.5 g in 1 POUCH
1651414-400-16100 POUCH in 1 BOTTLE (51414-400-16) / 2.5 g in 1 POUCH
1751414-400-171 POUCH in 1 PACKAGE (51414-400-17) / 3 g in 1 POUCH
1851414-400-182 POUCH in 1 PACKAGE (51414-400-18) / 3 g in 1 POUCH
1951414-400-193 POUCH in 1 PACKAGE (51414-400-19) / 3 g in 1 POUCH
2051414-400-204 POUCH in 1 PACKAGE (51414-400-20) / 3 g in 1 POUCH
2151414-400-215 POUCH in 1 PACKAGE (51414-400-21) / 3 g in 1 POUCH
2251414-400-2210 POUCH in 1 PACKAGE (51414-400-22) / 4 g in 1 POUCH
2351414-400-2315 POUCH in 1 PACKAGE (51414-400-23) / 4 g in 1 POUCH
2451414-400-2420 POUCH in 1 PACKAGE (51414-400-24) / 4 g in 1 POUCH
2551414-400-2525 POUCH in 1 PACKAGE (51414-400-25) / 4 g in 1 POUCH
2651414-400-2630 POUCH in 1 PACKAGE (51414-400-26) / 4 g in 1 POUCH
2751414-400-2735 POUCH in 1 PACKAGE (51414-400-27) / 4 g in 1 POUCH
2851414-400-2840 POUCH in 1 PACKAGE (51414-400-28) / 4 g in 1 POUCH
2951414-400-2945 POUCH in 1 PACKAGE (51414-400-29) / 4 g in 1 POUCH
3051414-400-3050 POUCH in 1 PACKAGE (51414-400-30) / 4 g in 1 POUCH
3151414-400-3155 POUCH in 1 PACKAGE (51414-400-31) / 4 g in 1 POUCH
3251414-400-3260 POUCH in 1 PACKAGE (51414-400-32) / 4 g in 1 POUCH
3351414-400-3365 POUCH in 1 PACKAGE (51414-400-33) / 4 g in 1 POUCH
3451414-400-3470 POUCH in 1 PACKAGE (51414-400-34) / 4 g in 1 POUCH
3551414-400-3575 POUCH in 1 PACKAGE (51414-400-35) / 4 g in 1 POUCH
3651414-400-3680 POUCH in 1 PACKAGE (51414-400-36) / 4 g in 1 POUCH
3751414-400-3785 POUCH in 1 PACKAGE (51414-400-37) / 4 g in 1 POUCH
3851414-400-3890 POUCH in 1 PACKAGE (51414-400-38) / 4 g in 1 POUCH
3951414-400-3995 POUCH in 1 PACKAGE (51414-400-39) / 4 g in 1 POUCH
4051414-400-40100 POUCH in 1 PACKAGE (51414-400-40) / 4 g in 1 POUCH
4151414-400-4116 POUCH in 1 BOTTLE (51414-400-41) / 3 g in 1 POUCH
4251414-400-4260 POUCH in 1 BOTTLE (51414-400-42) / 3 g in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC51414-400The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEantibacterial wet wipesThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBenzalkonium ChlorideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESWABThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE5/8/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERpart333AThis corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEYuyao Jessie Commodity Co.,Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEBENZALKONIUM CHLORIDEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH.13 
ACTIVE INGRED UNITg/100g 

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This page was last updated on: 2/1/2023