74542-013 NDC - WELKIN ALCOHOL WIPES ()

Drug Information

  • Product NDC: 74542-013
  • Proprietary Name: Welkin alcohol wipes
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Ningbo SKL International Co.,Ltd.
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:5/30/2020

Package Information

No. Package Code Package Description Billing Unit
174542-013-0150 BOX in 1 PACKAGE (74542-013-01) / 135 mL in 1 BOX
274542-013-0255 BOX in 1 PACKAGE (74542-013-02) / 135 mL in 1 BOX
374542-013-0360 BOX in 1 PACKAGE (74542-013-03) / 135 mL in 1 BOX
474542-013-0465 BOX in 1 PACKAGE (74542-013-04) / 135 mL in 1 BOX
574542-013-0570 BOX in 1 PACKAGE (74542-013-05) / 135 mL in 1 BOX
674542-013-06135 BOX in 1 PACKAGE (74542-013-06) / 135 mL in 1 BOX
774542-013-0780 BOX in 1 PACKAGE (74542-013-07) / 135 mL in 1 BOX
874542-013-0885 BOX in 1 PACKAGE (74542-013-08) / 135 mL in 1 BOX
974542-013-0980 BOX in 1 PACKAGE (74542-013-09) / 135 mL in 1 BOX
1074542-013-1095 BOX in 1 PACKAGE (74542-013-10) / 135 mL in 1 BOX
1174542-013-11100 BOX in 1 PACKAGE (74542-013-11) / 135 mL in 1 BOX
1274542-013-12105 BOX in 1 PACKAGE (74542-013-12) / 135 mL in 1 BOX
1374542-013-13110 BOX in 1 PACKAGE (74542-013-13) / 135 mL in 1 BOX
1474542-013-14115 BOX in 1 PACKAGE (74542-013-14) / 135 mL in 1 BOX
1574542-013-15120 BOX in 1 PACKAGE (74542-013-15) / 135 mL in 1 BOX
1674542-013-16125 BOX in 1 PACKAGE (74542-013-16) / 135 mL in 1 BOX
1774542-013-17130 BOX in 1 PACKAGE (74542-013-17) / 135 mL in 1 BOX
1874542-013-19140 BOX in 1 PACKAGE (74542-013-19) / 135 mL in 1 BOX
1974542-013-20145 BOX in 1 PACKAGE (74542-013-20) / 135 mL in 1 BOX
2074542-013-21150 BOX in 1 PACKAGE (74542-013-21) / 135 mL in 1 BOX
2174542-013-22155 BOX in 1 PACKAGE (74542-013-22) / 135 mL in 1 BOX
2274542-013-23160 BOX in 1 PACKAGE (74542-013-23) / 135 mL in 1 BOX
2374542-013-24165 BOX in 1 PACKAGE (74542-013-24) / 135 mL in 1 BOX
2474542-013-25170 BOX in 1 PACKAGE (74542-013-25) / 135 mL in 1 BOX
2574542-013-26175 BOX in 1 PACKAGE (74542-013-26) / 135 mL in 1 BOX
2674542-013-27180 BOX in 1 PACKAGE (74542-013-27) / 135 mL in 1 BOX
2774542-013-28185 BOX in 1 PACKAGE (74542-013-28) / 135 mL in 1 BOX
2874542-013-29190 BOX in 1 PACKAGE (74542-013-29) / 135 mL in 1 BOX
2974542-013-30195 BOX in 1 PACKAGE (74542-013-30) / 135 mL in 1 BOX
3074542-013-31200 BOX in 1 PACKAGE (74542-013-31) / 135 mL in 1 BOX
3174542-013-32250 BOX in 1 PACKAGE (74542-013-32) / 135 mL in 1 BOX
3274542-013-33300 BOX in 1 PACKAGE (74542-013-33) / 135 mL in 1 BOX
3374542-013-3475 BOX in 1 PACKAGE (74542-013-34) / 135 mL in 1 BOX

NDC Record

Field Name Field Value Definition
PRODUCT NDC74542-013The 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.
PROPRIETARY NAMEWelkin alcohol wipesThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/30/2020This 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 NAMENingbo SKL International Co.,Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/25/2025

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