79805-001 NDC - HAND SANITIZER

Drug Information

Product NDC: 79805-001
Proprietary Name: HAND SANITIZER
Non Proprietary Name: HAND SANITIZER
Active Ingredient(s): 68 mL/100mL ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): GEL

Labeler Information

Field Name	Field Value
Labeler Name:	JUXIN (Jiangsu) New Material Packaging Co., Ltd.
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED DRUG OTHER
Start Marketing Date:	3/30/2020

Package Information

No.	Package Code	Package Description	Billing Unit
1	79805-001-01	60 mL in 1 BOTTLE (79805-001-01)
2	79805-001-02	120 mL in 1 BOTTLE (79805-001-02)
3	79805-001-03	300 mL in 1 BOTTLE (79805-001-03)
4	79805-001-04	500 mL in 1 BOTTLE (79805-001-04)
5	79805-001-05	3800 mL in 1 BOTTLE (79805-001-05)
6	79805-001-06	90 mL in 1 BOTTLE (79805-001-06)
7	79805-001-07	100 mL in 1 BOTTLE (79805-001-07)
8	79805-001-08	750 mL in 1 BOTTLE (79805-001-08)
9	79805-001-09	1000 mL in 1 BOTTLE (79805-001-09)
10	79805-001-10	18 mL in 1 BOTTLE (79805-001-10)
11	79805-001-11	250 mL in 1 BOTTLE (79805-001-11)
12	79805-001-12	2000 mL in 1 BOTTLE (79805-001-12)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	79805-001	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.
PRODUCT TYPE NAME	HUMAN OTC DRUG	Name of Company corresponding to the labeler code segment of the Product NDC.
PROPRIETARY NAME	HAND SANITIZER	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAME	HAND SANITIZER	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	GEL	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	TOPICAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	3/30/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED DRUG OTHER	Product 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.
LABELER NAME	JUXIN (Jiangsu) New Material Packaging Co., Ltd.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	ALCOHOL	An 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 STRENGTH	68
ACTIVE INGRED UNIT	mL/100mL

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This page was last updated on: 12/19/2025

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