73905-001 NDC - HAND SANITIZER (ISOPROPYL ALCOHOL)

Drug Information

Product NDC: 73905-001

Proprietary Name: Hand Sanitizer

Non Proprietary Name: ISOPROPYL ALCOHOL

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


Administration Route(s): TOPICAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/28/2020

Package Information

No. Package Code Package Description Billing Unit
173905-001-01100 mL in 1 BOTTLE (73905-001-01)
273905-001-0220 mL in 1 BOTTLE (73905-001-02)
373905-001-0330 mL in 1 BOTTLE (73905-001-03)
473905-001-0455 mL in 1 BOTTLE (73905-001-04)
573905-001-0560 mL in 1 BOTTLE (73905-001-05)
673905-001-0680 mL in 1 BOTTLE (73905-001-06)
773905-001-07120 mL in 1 BOTTLE (73905-001-07)
873905-001-08200 mL in 1 BOTTLE (73905-001-08)
973905-001-09236 mL in 1 BOTTLE (73905-001-09)
1073905-001-10260 mL in 1 BOTTLE (73905-001-10)
1173905-001-11300 mL in 1 BOTTLE (73905-001-11)
1273905-001-12500 mL in 1 BOTTLE (73905-001-12)
1373905-001-13560 mL in 1 BOTTLE (73905-001-13)
1473905-001-14980 mL in 1 BOTTLE (73905-001-14)
1573905-001-15985 mL in 1 BOTTLE (73905-001-15)
1673905-001-162000 mL in 1 BOTTLE (73905-001-16)
1773905-001-173000 mL in 1 BOTTLE (73905-001-17)
1873905-001-184000 mL in 1 BOTTLE (73905-001-18)
1973905-001-195000 mL in 1 BOTTLE (73905-001-19)
2073905-001-2020000 mL in 1 BOTTLE (73905-001-20)
2173905-001-2125000 mL in 1 BOTTLE (73905-001-21)
2273905-001-2250000 mL in 1 BOTTLE (73905-001-22)
2373905-001-23200000 mL in 1 BOTTLE (73905-001-23)
2473905-001-241000000 mL in 1 BOTTLE (73905-001-24)
2573905-001-25750 mL in 1 BOTTLE (73905-001-25)
2673905-001-2610 mL in 1 BOTTLE (73905-001-26)
2773905-001-2745 mL in 1 BOTTLE (73905-001-27)
2873905-001-28180 mL in 1 BOTTLE (73905-001-28)
2973905-001-29240 mL in 1 BOTTLE (73905-001-29)
3073905-001-30250 mL in 1 BOTTLE (73905-001-30)
3173905-001-31350 mL in 1 BOTTLE (73905-001-31)
3273905-001-32400 mL in 1 BOTTLE (73905-001-32)
3373905-001-33600 mL in 1 BOTTLE (73905-001-33)
3473905-001-34900 mL in 1 BOTTLE (73905-001-34)
3573905-001-351000 mL in 1 BOTTLE (73905-001-35)
3673905-001-361500 mL in 1 BOTTLE (73905-001-36)
3773905-001-372500 mL in 1 BOTTLE (73905-001-37)
3873905-001-3810000 mL in 1 BOTTLE (73905-001-38)
3973905-001-3945000 mL in 1 BOTTLE (73905-001-39)
4073905-001-40100000 mL in 1 BOTTLE (73905-001-40)
4173905-001-41500000 mL in 1 BOTTLE (73905-001-41)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73905-001The 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.
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 NAMEHand SanitizerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEISOPROPYL ALCOHOLThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe 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 DATE3/28/2020This 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 NAMEZHEJIANG JINGHUI COSMETICS SHARE CO.,LTDName 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 STRENGTH70 
ACTIVE INGRED UNITmL/100mL 

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