73905-002 NDC - 75% ALCOHOL DISNFECTANT ()

Drug Information

  • Product NDC: 73905-002
  • Proprietary Name: 75% ALCOHOL DISNFECTANT
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/30/2020
End Marketing Date:5/3/2020

Package Information

No. Package Code Package Description Billing Unit
173905-002-01100 mL in 1 BOTTLE (73905-002-01)
273905-002-0220 mL in 1 BOTTLE (73905-002-02)
373905-002-0330 mL in 1 BOTTLE (73905-002-03)
473905-002-0455 mL in 1 BOTTLE (73905-002-04)
573905-002-0560 mL in 1 BOTTLE (73905-002-05)
673905-002-0680 mL in 1 BOTTLE (73905-002-06)
773905-002-07120 mL in 1 BOTTLE (73905-002-07)
873905-002-08200 mL in 1 BOTTLE (73905-002-08)
973905-002-09236 mL in 1 BOTTLE (73905-002-09)
1073905-002-10260 mL in 1 BOTTLE (73905-002-10)
1173905-002-11300 mL in 1 BOTTLE (73905-002-11)
1273905-002-12500 mL in 1 BOTTLE (73905-002-12)
1373905-002-13560 mL in 1 BOTTLE (73905-002-13)
1473905-002-14980 mL in 1 BOTTLE (73905-002-14)
1573905-002-15985 mL in 1 BOTTLE (73905-002-15)
1673905-002-16300 mL in 1 BOTTLE (73905-002-16)
1773905-002-174000 mL in 1 BOTTLE (73905-002-17)
1873905-002-182000 mL in 1 BOTTLE (73905-002-18)
1973905-002-193000 mL in 1 BOTTLE (73905-002-19)
2073905-002-205000 mL in 1 BOTTLE (73905-002-20)
2173905-002-2125000 mL in 1 BOTTLE (73905-002-21)
2273905-002-2250000 mL in 1 BOTTLE (73905-002-22)
2373905-002-2320000 mL in 1 BOTTLE (73905-002-23)
2473905-002-241000000 mL in 1 BOTTLE (73905-002-24)
2573905-002-25750 mL in 1 BOTTLE (73905-002-25)
2673905-002-262000 mL in 1 BOTTLE (73905-002-26)
2773905-002-2710 mL in 1 BOTTLE (73905-002-27)
2873905-002-2710 mL in 1 BOTTLE (73905-002-27)
2973905-002-2845 mL in 1 BOTTLE (73905-002-28)
3073905-002-2845 mL in 1 BOTTLE (73905-002-28)
3173905-002-29180 mL in 1 BOTTLE (73905-002-29)
3273905-002-29180 mL in 1 BOTTLE (73905-002-29)
3373905-002-30240 mL in 1 BOTTLE (73905-002-30)
3473905-002-30240 mL in 1 BOTTLE (73905-002-30)
3573905-002-31250 mL in 1 BOTTLE (73905-002-31)
3673905-002-31250 mL in 1 BOTTLE (73905-002-31)
3773905-002-32350 mL in 1 BOTTLE (73905-002-32)
3873905-002-32350 mL in 1 BOTTLE (73905-002-32)
3973905-002-33400 mL in 1 BOTTLE (73905-002-33)
4073905-002-33400 mL in 1 BOTTLE (73905-002-33)
4173905-002-34600 mL in 1 BOTTLE (73905-002-34)
4273905-002-34600 mL in 1 BOTTLE (73905-002-34)
4373905-002-35900 mL in 1 BOTTLE (73905-002-35)
4473905-002-35900 mL in 1 BOTTLE (73905-002-35)
4573905-002-361000 mL in 1 BOTTLE (73905-002-36)
4673905-002-361000 mL in 1 BOTTLE (73905-002-36)
4773905-002-371500 mL in 1 BOTTLE (73905-002-37)
4873905-002-371500 mL in 1 BOTTLE (73905-002-37)
4973905-002-382500 mL in 1 BOTTLE (73905-002-38)
5073905-002-382500 mL in 1 BOTTLE (73905-002-38)
5173905-002-3910000 mL in 1 BOTTLE (73905-002-39)
5273905-002-3910000 mL in 1 BOTTLE (73905-002-39)
5373905-002-4045000 mL in 1 BOTTLE (73905-002-40)
5473905-002-4045000 mL in 1 BOTTLE (73905-002-40)
5573905-002-41100000 mL in 1 BOTTLE (73905-002-41)
5673905-002-41100000 mL in 1 BOTTLE (73905-002-41)
5773905-002-42500000 mL in 1 BOTTLE (73905-002-42)
5873905-002-42500000 mL in 1 BOTTLE (73905-002-42)
5973905-002-43100 mL in 1 BOTTLE (73905-002-43)
6073905-002-43100 mL in 1 BOTTLE (73905-002-43)
6173905-002-4420 mL in 1 BOTTLE (73905-002-44)
6273905-002-4420 mL in 1 BOTTLE (73905-002-44)
6373905-002-4530 mL in 1 BOTTLE (73905-002-45)
6473905-002-4530 mL in 1 BOTTLE (73905-002-45)
6573905-002-4655 mL in 1 BOTTLE (73905-002-46)
6673905-002-4655 mL in 1 BOTTLE (73905-002-46)
6773905-002-4760 mL in 1 BOTTLE (73905-002-47)
6873905-002-4760 mL in 1 BOTTLE (73905-002-47)
6973905-002-4880 mL in 1 BOTTLE (73905-002-48)
7073905-002-4880 mL in 1 BOTTLE (73905-002-48)
7173905-002-49120 mL in 1 BOTTLE (73905-002-49)
7273905-002-49120 mL in 1 BOTTLE (73905-002-49)
7373905-002-50200 mL in 1 BOTTLE (73905-002-50)
7473905-002-50200 mL in 1 BOTTLE (73905-002-50)
7573905-002-51236 mL in 1 BOTTLE (73905-002-51)
7673905-002-51236 mL in 1 BOTTLE (73905-002-51)
7773905-002-52260 mL in 1 BOTTLE (73905-002-52)
7873905-002-52260 mL in 1 BOTTLE (73905-002-52)
7973905-002-53300 mL in 1 BOTTLE (73905-002-53)
8073905-002-53300 mL in 1 BOTTLE (73905-002-53)
8173905-002-54500 mL in 1 BOTTLE (73905-002-54)
8273905-002-54500 mL in 1 BOTTLE (73905-002-54)
8373905-002-55560 mL in 1 BOTTLE (73905-002-55)
8473905-002-55560 mL in 1 BOTTLE (73905-002-55)
8573905-002-56980 mL in 1 BOTTLE (73905-002-56)
8673905-002-56980 mL in 1 BOTTLE (73905-002-56)
8773905-002-57985 mL in 1 BOTTLE (73905-002-57)
8873905-002-57985 mL in 1 BOTTLE (73905-002-57)
8973905-002-58300 mL in 1 BOTTLE (73905-002-58)
9073905-002-58300 mL in 1 BOTTLE (73905-002-58)
9173905-002-594000 mL in 1 BOTTLE (73905-002-59)
9273905-002-594000 mL in 1 BOTTLE (73905-002-59)
9373905-002-602000 mL in 1 BOTTLE (73905-002-60)
9473905-002-602000 mL in 1 BOTTLE (73905-002-60)
9573905-002-613000 mL in 1 BOTTLE (73905-002-61)
9673905-002-613000 mL in 1 BOTTLE (73905-002-61)
9773905-002-625000 mL in 1 BOTTLE (73905-002-62)
9873905-002-625000 mL in 1 BOTTLE (73905-002-62)
9973905-002-6325000 mL in 1 BOTTLE (73905-002-63)
10073905-002-6325000 mL in 1 BOTTLE (73905-002-63)
10173905-002-6450000 mL in 1 BOTTLE (73905-002-64)
10273905-002-6450000 mL in 1 BOTTLE (73905-002-64)
10373905-002-6520000 mL in 1 BOTTLE (73905-002-65)
10473905-002-6520000 mL in 1 BOTTLE (73905-002-65)
10573905-002-661000000 mL in 1 BOTTLE (73905-002-66)
10673905-002-661000000 mL in 1 BOTTLE (73905-002-66)
10773905-002-67750 mL in 1 BOTTLE (73905-002-67)
10873905-002-67750 mL in 1 BOTTLE (73905-002-67)
10973905-002-682000 mL in 1 BOTTLE (73905-002-68)
11073905-002-682000 mL in 1 BOTTLE (73905-002-68)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73905-002The 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 NAME75% ALCOHOL DISNFECTANTThe 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.
END MARKETING DATE4/23/2024This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBER505G(a)(3)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.
LABELER NAMEZHEJIANG JINGHUI COSMETICS SHARE CO.,LTDName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC73905-002The 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 NAME75% ALCOHOL DISNFECTANTThe 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.
END MARKETING DATE4/23/2024This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBER505G(a)(3)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.
LABELER NAMEZHEJIANG JINGHUI COSMETICS SHARE CO.,LTDName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC73905-002The 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 NAME75% ALCOHOL DISNFECTANTThe 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.
END MARKETING DATE5/3/2020This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
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.

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This page was last updated on: 6/6/2025

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