73760-003 NDC - ALCOHOL WET WIPES (ALCOHOL)

Drug Information

Product NDC: 73760-003

Proprietary Name: Alcohol Wet Wipes

Non Proprietary Name: Alcohol

Active Ingredient(s):
  • 70 g/100g ALCOHOL


Administration Route(s): TOPICAL

Dosage Form(s): CLOTH

Labeler Information

Labeler Name: Zhejiang Easyclean Daily Chemical Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:5/29/2020

Package Information

No. Package Code Package Description Billing Unit
173760-003-01100 BAG in 1 CARTON (73760-003-01) / 10 POUCH in 1 BAG / 23 g in 1 POUCH
273760-003-02100 BAG in 1 CARTON (73760-003-02) / 15 POUCH in 1 BAG / 35 g in 1 POUCH
373760-003-0348 BAG in 1 CARTON (73760-003-03) / 30 POUCH in 1 BAG / 71 g in 1 POUCH
473760-003-0448 BAG in 1 CARTON (73760-003-04) / 48 POUCH in 1 BAG / 57 g in 1 POUCH
573760-003-0548 BAG in 1 CARTON (73760-003-05) / 48 POUCH in 1 BAG / 119 g in 1 POUCH
673760-003-0612 BAG in 1 CARTON (73760-003-06) / 80 POUCH in 1 BAG / 190 g in 1 POUCH
773760-003-07100 PAIL in 1 CARTON (73760-003-07) / 30 POUCH in 1 PAIL / 22 g in 1 POUCH
873760-003-0818 PAIL in 1 CARTON (73760-003-08) / 100 POUCH in 1 PAIL / 136 g in 1 POUCH
973760-003-0924 BAG in 1 CARTON (73760-003-09) / 50 POUCH in 1 BAG / 119 g in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC73760-003The 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 NAMEAlcohol 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 NAMEAlcoholThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECLOTHThe 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 DATE5/29/2020This 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 NAMEZhejiang Easyclean Daily Chemical Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALCOHOLAn 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 STRENGTH70 
ACTIVE INGRED UNITg/100g 

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