61312-001 NDC - HAND SANITIZING WIPES ()

Drug Information

  • Product NDC: 61312-001
  • Proprietary Name: Hand Sanitizing wipes
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: HANGZHOU GUOGUANG TOURING COMMODITY CO., LTD.
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/14/2013

Package Information

No. Package Code Package Description Billing Unit
161312-001-0110 POUCH in 1 BOTTLE (61312-001-01) / .00468 g in 1 POUCH
261312-001-0225 POUCH in 1 BOTTLE (61312-001-02) / .00468 g in 1 POUCH
361312-001-0340 POUCH in 1 BOTTLE (61312-001-03) / .00468 g in 1 POUCH
461312-001-0460 POUCH in 1 BOTTLE (61312-001-04) / .00468 g in 1 POUCH
561312-001-05100 POUCH in 1 BOTTLE (61312-001-05) / .00468 g in 1 POUCH
661312-001-06120 POUCH in 1 BOTTLE (61312-001-06) / .00468 g in 1 POUCH
761312-001-07200 POUCH in 1 BOTTLE (61312-001-07) / .00468 g in 1 POUCH
861312-001-08240 POUCH in 1 BOTTLE (61312-001-08) / .00468 g in 1 POUCH
961312-001-09250 POUCH in 1 BOTTLE (61312-001-09) / .00468 g in 1 POUCH
1061312-001-10800 POUCH in 1 BOTTLE (61312-001-10) / .00468 g in 1 POUCH
1161312-001-111200 POUCH in 1 BOTTLE (61312-001-11) / .00468 g in 1 POUCH
1261312-001-121500 POUCH in 1 BOTTLE (61312-001-12) / .00468 g in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC61312-001The 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 NAMEHand Sanitizing 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 DATE3/14/2013This 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 NAMEHANGZHOU GUOGUANG TOURING COMMODITY 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: 12/19/2025

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