76591-101 NDC - RINSE-FREE HAND SANITIZER ()

Drug Information

  • Product NDC: 76591-101
  • Proprietary Name: Rinse-free Hand Sanitizer
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Guangzhou Gotdya Fine Chemical 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
176591-101-0130 mL in 1 BOTTLE (76591-101-01)
276591-101-0250 mL in 1 BOTTLE (76591-101-02)
376591-101-0360 mL in 1 BOTTLE (76591-101-03)
476591-101-0480 mL in 1 BOTTLE (76591-101-04)
576591-101-05100 mL in 1 BOTTLE (76591-101-05)
676591-101-06120 mL in 1 BOTTLE (76591-101-06)
776591-101-07150 mL in 1 BOTTLE (76591-101-07)
876591-101-08200 mL in 1 BOTTLE (76591-101-08)
976591-101-09240 mL in 1 BOTTLE (76591-101-09)
1076591-101-10300 mL in 1 BOTTLE (76591-101-10)
1176591-101-11350 mL in 1 BOTTLE (76591-101-11)
1276591-101-12380 mL in 1 BOTTLE (76591-101-12)
1376591-101-13400 mL in 1 BOTTLE (76591-101-13)
1476591-101-14420 mL in 1 BOTTLE (76591-101-14)
1576591-101-15450 mL in 1 BOTTLE (76591-101-15)
1676591-101-16500 mL in 1 BOTTLE (76591-101-16)
1776591-101-17600 mL in 1 BOTTLE (76591-101-17)
1876591-101-18750 mL in 1 BOTTLE (76591-101-18)
1976591-101-191000 mL in 1 BOTTLE (76591-101-19)
2076591-101-202500 mL in 1 BOTTLE (76591-101-20)
2176591-101-213000 mL in 1 BOTTLE (76591-101-21)
2276591-101-223785 mL in 1 BOTTLE (76591-101-22)
2376591-101-234500 mL in 1 BOTTLE (76591-101-23)
2476591-101-245000 mL in 1 BOTTLE (76591-101-24)
2576591-101-2510000 mL in 1 BOTTLE (76591-101-25)
2676591-101-2625000 mL in 1 BOTTLE (76591-101-26)
2776591-101-2750000 mL in 1 BOTTLE (76591-101-27)

NDC Record

Field Name Field Value Definition
PRODUCT NDC76591-101The 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 NAMERinse-free Hand SanitizerThe 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 NAMEGuangzhou Gotdya Fine Chemical 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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