79481-0156 NDC - MEIJER ANTIBACTERIAL AMBER HAND (BENZALKONIUM CHLORIDE)

Drug Information

Product NDC: 79481-0156
Proprietary Name: Meijer Antibacterial Amber Hand
Non Proprietary Name: Benzalkonium Chloride
Active Ingredient(s): .13 g/100mL BENZALKONIUM CHLORIDE
Administration Route(s): TOPICAL
Dosage Form(s): SOAP

Labeler Information

Field Name	Field Value
Labeler Name:	Meijer, Inc.
Product Type:	HUMAN OTC DRUG
FDA Application Number:	505G(a)(3)
Marketing Category:	OTC MONOGRAPH DRUG
Start Marketing Date:	12/5/2024

Package Information

No.	Package Code	Package Description	Billing Unit
1	79481-0156-1	1650 mL in 1 BOTTLE (79481-0156-1)
2	79481-0156-2	332 mL in 1 BOTTLE, PUMP (79481-0156-2)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	79481-0156	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.
PRODUCT TYPE NAME	HUMAN OTC DRUG	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.
PROPRIETARY NAME	Meijer Antibacterial Amber Hand	This is the date that the labeler indicates was the start of its marketing of the drug product.
NON PROPRIETARY NAME	Benzalkonium Chloride	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.
DOSAGE FORM NAME	SOAP	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.
ROUTE NAME	TOPICAL	Name of Company corresponding to the labeler code segment of the Product NDC.
START MARKETING DATE	12/5/2024	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.
MARKETING CATEGORY NAME	OTC MONOGRAPH DRUG
APPLICATION NUMBER	505G(a)(3)
LABELER NAME	Meijer, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	BENZALKONIUM CHLORIDE	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	.13
ACTIVE INGRED UNIT	g/100mL

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This page was last updated on: 12/6/2025

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