90042-101 NDC - ALCOHOL WET WIPE ()

Drug Information

  • Product NDC: 90042-101
  • Proprietary Name: Alcohol wet wipe
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Shandong mengyida daily necessities Co., Ltd.
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
190042-101-011 CLOTH in 1 BAG (90042-101-01)
290042-101-0210 CLOTH in 1 BAG (90042-101-02)
390042-101-0320 CLOTH in 1 BAG (90042-101-03)
490042-101-0450 CLOTH in 1 BAG (90042-101-04)
590042-101-0570 CLOTH in 1 BAG (90042-101-05)
690042-101-0680 CLOTH in 1 BAG (90042-101-06)
790042-101-07100 CLOTH in 1 BAG (90042-101-07)
890042-101-08120 CLOTH in 1 BAG (90042-101-08)
990042-101-0960 CLOTH in 1 CANISTER (90042-101-09)
1090042-101-1060 CLOTH in 1 CANISTER (90042-101-10)
1190042-101-1175 CLOTH in 1 CANISTER (90042-101-11)
1290042-101-1280 CLOTH in 1 CANISTER (90042-101-12)
1390042-101-13100 CLOTH in 1 CANISTER (90042-101-13)
1490042-101-14120 CLOTH in 1 CANISTER (90042-101-14)
1590042-101-15160 CLOTH in 1 CANISTER (90042-101-15)
1690042-101-16180 CLOTH in 1 CANISTER (90042-101-16)
1790042-101-17200 CLOTH in 1 CANISTER (90042-101-17)
1890042-101-18250 CLOTH in 1 CANISTER (90042-101-18)
1990042-101-19500 CLOTH in 1 CANISTER (90042-101-19)
2090042-101-20800 CLOTH in 1 CANISTER (90042-101-20)
2190042-101-2150 CLOTH in 1 CANISTER (90042-101-21)
2290042-101-221000 CLOTH in 1 CANISTER (90042-101-22)
2390042-101-231200 CLOTH in 1 CANISTER (90042-101-23)

NDC Record

Field Name Field Value Definition
PRODUCT NDC90042-101The 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 wet wipeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/30/2020This 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 NAMEShandong mengyida daily necessities 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: 12/6/2025

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