73905-015 NDC - HAND SANITIZER (ETHYL ALCOHOL)

Drug Information

Product NDC: 73905-015

Proprietary Name: Hand Sanitizer

Non Proprietary Name: Ethyl Alcohol

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


Administration Route(s): TOPICAL

Dosage Form(s): GEL

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:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
173905-015-012 mL in 1 BOTTLE (73905-015-01)
273905-015-025 mL in 1 BOTTLE (73905-015-02)
373905-015-0310 mL in 1 BOTTLE (73905-015-03)
473905-015-0420 mL in 1 BOTTLE (73905-015-04)
573905-015-0530 mL in 1 BOTTLE (73905-015-05)
673905-015-0645 mL in 1 BOTTLE (73905-015-06)
773905-015-0755 mL in 1 BOTTLE (73905-015-07)
873905-015-0860 mL in 1 BOTTLE (73905-015-08)
973905-015-0980 mL in 1 BOTTLE (73905-015-09)
1073905-015-10100 mL in 1 BOTTLE (73905-015-10)
1173905-015-11120 mL in 1 BOTTLE (73905-015-11)
1273905-015-12180 mL in 1 BOTTLE (73905-015-12)
1373905-015-13200 mL in 1 BOTTLE (73905-015-13)
1473905-015-14236 mL in 1 BOTTLE (73905-015-14)
1573905-015-15237 mL in 1 BOTTLE (73905-015-15)
1673905-015-16240 mL in 1 BOTTLE (73905-015-16)
1773905-015-17250 mL in 1 BOTTLE (73905-015-17)
1873905-015-18260 mL in 1 BOTTLE (73905-015-18)
1973905-015-19300 mL in 1 BOTTLE (73905-015-19)
2073905-015-20350 mL in 1 BOTTLE (73905-015-20)
2173905-015-21400 mL in 1 BOTTLE (73905-015-21)
2273905-015-22500 mL in 1 BOTTLE (73905-015-22)
2373905-015-23560 mL in 1 BOTTLE (73905-015-23)
2473905-015-24600 mL in 1 BOTTLE (73905-015-24)
2573905-015-25750 mL in 1 BOTTLE (73905-015-25)
2673905-015-26900 mL in 1 BOTTLE (73905-015-26)
2773905-015-27980 mL in 1 BOTTLE (73905-015-27)
2873905-015-28985 mL in 1 BOTTLE (73905-015-28)
2973905-015-291000 mL in 1 BOTTLE (73905-015-29)
3073905-015-301300 mL in 1 BOTTLE (73905-015-30)
3173905-015-311500 mL in 1 BOTTLE (73905-015-31)
3273905-015-321800 mL in 1 BOTTLE (73905-015-32)
3373905-015-332000 mL in 1 BOTTLE (73905-015-33)
3473905-015-342500 mL in 1 BOTTLE (73905-015-34)
3573905-015-353000 mL in 1 BOTTLE (73905-015-35)
3673905-015-363800 mL in 1 BOTTLE (73905-015-36)
3773905-015-374000 mL in 1 BOTTLE (73905-015-37)
3873905-015-385000 mL in 1 BOTTLE (73905-015-38)
3973905-015-3910000 mL in 1 BOTTLE (73905-015-39)
4073905-015-4020000 mL in 1 BOTTLE (73905-015-40)
4173905-015-4125000 mL in 1 BOTTLE (73905-015-41)
4273905-015-4245000 mL in 1 BOTTLE (73905-015-42)
4373905-015-4350000 mL in 1 BOTTLE (73905-015-43)
4473905-015-44100000 mL in 1 BOTTLE (73905-015-44)
4573905-015-45200000 mL in 1 BOTTLE (73905-015-45)
4673905-015-46500000 mL in 1 BOTTLE (73905-015-46)
4773905-015-471000000 mL in 1 BOTTLE (73905-015-47)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73905-015The 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 NAMEEthyl AlcoholThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEGELThe 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 DATE3/30/2020This 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 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