78149-001 NDC - HYNAUT ALCOHOL PREP PAD ()

Drug Information

Product NDC: 78149-001
Proprietary Name: Hynaut Alcohol Prep Pad
Non Proprietary Name:
Active Ingredient(s):
Administration Route(s):
Dosage Form(s):

Labeler Information

Field Name	Field Value
Labeler Name:	Qingdao Hainuo Biological Engineering Co., Ltd.
Product Type:
FDA Application Number:	part333A
Marketing Category:	OTC MONOGRAPH NOT FINAL
Start Marketing Date:	6/23/2020
End Marketing Date:	6/23/2020

Package Information

No.	Package Code	Package Description	Billing Unit
1	78149-001-01	1 PATCH in 1 PACKAGE (78149-001-01) / 2.7 g in 1 PATCH
2	78149-001-02	100 PATCH in 1 BOX (78149-001-02) / .7 g in 1 PATCH (78149-001-01)
3	78149-001-04	100 PATCH in 1 BOX (78149-001-04) / 1.05 g in 1 PATCH (78149-001-03)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	78149-001	The 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 NAME	Alcohol Prep Pads	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	5/20/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	6/4/2020	This 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 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	Qingdao Hainuo Biological Engineering Co., Ltd.	Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC	78149-001	The 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 NAME	Hynaut Alcohol Prep Pad	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	6/23/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	6/23/2020	This 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 NAME	OTC MONOGRAPH NOT FINAL	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	Qingdao Hainuo Biological Engineering 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: 1/16/2026

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