75749-051 NDC - ALCOHOL WIPES ()

Drug Information

  • Product NDC: 75749-051
  • Proprietary Name: ALCOHOL WIPES
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Ningbo Pretty Tourism Manufacture Co., Ltd
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:8/11/2020

Package Information

No. Package Code Package Description Billing Unit
175749-051-011 CONTAINER in 1 CONTAINER (75749-051-01) / 5 mL in 1 CONTAINER
275749-051-022 CONTAINER in 1 CONTAINER (75749-051-02) / 10 mL in 1 CONTAINER
375749-051-0310 CONTAINER in 1 CONTAINER (75749-051-03) / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
475749-051-0412 CONTAINER in 1 CONTAINER (75749-051-04) / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
575749-051-0520 CONTAINER in 1 CONTAINER (75749-051-05) / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
675749-051-0624 CONTAINER in 1 CONTAINER (75749-051-06) / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
775749-051-0730 CONTAINER in 1 CONTAINER (75749-051-07) / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
875749-051-0840 CONTAINER in 1 CONTAINER (75749-051-08) / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
975749-051-0948 CONTAINER in 1 CONTAINER (75749-051-09) / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
1075749-051-1050 CONTAINER in 1 CONTAINER (75749-051-10) / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
1175749-051-11100 CONTAINER in 1 CONTAINER (75749-051-11) / 1 CONTAINER in 1 CONTAINER / 5 mL in 1 CONTAINER
1275749-051-1210 CONTAINER in 1 CONTAINER (75749-051-12) / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
1375749-051-1312 CONTAINER in 1 CONTAINER (75749-051-13) / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
1475749-051-1420 CONTAINER in 1 CONTAINER (75749-051-14) / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
1575749-051-1524 CONTAINER in 1 CONTAINER (75749-051-15) / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
1675749-051-1630 CONTAINER in 1 CONTAINER (75749-051-16) / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
1775749-051-1740 CONTAINER in 1 CONTAINER (75749-051-17) / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
1875749-051-1848 CONTAINER in 1 CONTAINER (75749-051-18) / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
1975749-051-1950 CONTAINER in 1 CONTAINER (75749-051-19) / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER
2075749-051-20100 CONTAINER in 1 CONTAINER (75749-051-20) / 2 CONTAINER in 1 CONTAINER / 10 mL in 1 CONTAINER

NDC Record

Field Name Field Value Definition
PRODUCT NDC75749-051The 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 NAMEALCOHOL 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 DATE8/11/2020This 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 Pretty Tourism Manufacture Co., LtdName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 1/2/2026

Previous Code
Next Code