78691-004 NDC - BIOPURE ANTIBACTERIAL HAND WIPE ()

Drug Information

  • Product NDC: 78691-004
  • Proprietary Name: Biopure antibacterial hand wipe
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: QUEST USA CORP.
Product Type:
FDA Application Number: 505G(a)(3)
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:9/15/2020

Package Information

No. Package Code Package Description Billing Unit
178691-004-001600 PATCH in 1 BAG (78691-004-00) / 3.44 mL in 1 PATCH
278691-004-01800 PATCH in 1 BAG (78691-004-01) / 3.25 mL in 1 PATCH
378691-004-0250 PATCH in 1 POUCH (78691-004-02) / 5.7 mL in 1 PATCH
478691-004-03100 PATCH in 1 CANISTER (78691-004-03) / 5.37 mL in 1 PATCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC78691-004The 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 NAMEBiopure antibacterial hand 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 DATE9/15/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBER505G(a)(3)This 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 NAMEQUEST USA CORP.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/21/2025

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