75109-005 NDC - WET WIPE (ALCOHOL)

Drug Information

Product NDC: 75109-005

Proprietary Name: Wet Wipe

Non Proprietary Name: Alcohol

Active Ingredient(s):
  • 75 mL/100mL ALCOHOL


Administration Route(s): TOPICAL

Dosage Form(s): CLOTH

Labeler Information

Labeler Name: Kangna (Zhejiang) Medical Supplies Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/21/2020

Package Information

No. Package Code Package Description Billing Unit
175109-005-01100 POUCH in 1 BOX (75109-005-01) / 6.5 mL in 1 POUCH
275109-005-0250 POUCH in 1 BOX (75109-005-02) / 2.8 mL in 1 POUCH
375109-005-035 POUCH in 1 PACKAGE (75109-005-03) / 18.9 mL in 1 POUCH
475109-005-0410 POUCH in 1 PACKAGE (75109-005-04) / 37.8 mL in 1 POUCH
575109-005-0525 POUCH in 1 PACKAGE (75109-005-05) / 94.5 mL in 1 POUCH
675109-005-0625 POUCH in 1 PACKAGE (75109-005-06) / 189 mL in 1 POUCH
775109-005-0730 PACKAGE in 1 CASE (75109-005-07) / 189 mL in 1 PACKAGE
875109-005-0850 POUCH in 1 PACKAGE (75109-005-08) / 302.4 mL in 1 POUCH
975109-005-0980 POUCH in 1 PACKAGE (75109-005-09) / 378 mL in 1 POUCH
1075109-005-1040 POUCH in 1 CANISTER (75109-005-10) / 181.44 mL in 1 POUCH
1175109-005-11100 POUCH in 1 CONTAINER (75109-005-11) / 408.24 mL in 1 POUCH
1275109-005-15150 POUCH in 1 CONTAINER (75109-005-15) / 235.2 mL in 1 POUCH
1375109-005-16160 POUCH in 1 CONTAINER (75109-005-16) / 333.8496 mL in 1 POUCH
1475109-005-21100 POUCH in 1 BOX (75109-005-21) / 2 mL in 1 POUCH
1575109-005-2250 POUCH in 1 BOX (75109-005-22) / 2.8 mL in 1 POUCH
1675109-005-235 POUCH in 1 PACKAGE (75109-005-23) / 18.9 mL in 1 POUCH
1775109-005-2410 POUCH in 1 PACKAGE (75109-005-24) / 37.8 mL in 1 POUCH
1875109-005-2525 POUCH in 1 PACKAGE (75109-005-25) / 94.5 mL in 1 POUCH
1975109-005-2650 POUCH in 1 PACKAGE (75109-005-26) / 189 mL in 1 POUCH
2075109-005-2750 PACKAGE in 1 CASE (75109-005-27) / 24 POUCH in 1 PACKAGE / 189 mL in 1 POUCH
2175109-005-2880 POUCH in 1 PACKAGE (75109-005-28) / 302.4 mL in 1 POUCH
2275109-005-29100 POUCH in 1 PACKAGE (75109-005-29) / 378 mL in 1 POUCH
2375109-005-3040 POUCH in 1 CANISTER (75109-005-30) / 181.44 mL in 1 POUCH
2475109-005-31100 POUCH in 1 CANISTER (75109-005-31) / 408.24 mL in 1 POUCH
2575109-005-3270 POUCH in 1 CANISTER (75109-005-32) / 126.224 mL in 1 POUCH
2675109-005-3370 POUCH in 1 CANISTER (75109-005-33) / 141.12 mL in 1 POUCH
2775109-005-34100 POUCH in 1 CANISTER (75109-005-34) / 272.16 mL in 1 POUCH
2875109-005-35150 POUCH in 1 CANISTER (75109-005-35) / 235.2 mL in 1 POUCH
2975109-005-36160 POUCH in 1 CANISTER (75109-005-36) / 333.8496 mL in 1 POUCH
3075109-005-37100 POUCH in 1 CANISTER (75109-005-37) / 186.2 mL in 1 POUCH
3175109-005-38800 POUCH in 1 PACKAGE (75109-005-38) / 1515.136 mL in 1 POUCH
3275109-005-391200 POUCH in 1 PACKAGE (75109-005-39) / 2272.704 mL in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC75109-005The 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 NAMEWet WipeThe 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 DATE3/21/2020This 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 NAMEKangna (Zhejiang) Medical Supplies 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 STRENGTH75 
ACTIVE INGRED UNITmL/100mL 

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