74542-012 NDC - PURIDENE ()

Drug Information

Field Name	Field Value
Labeler Name:	Ningbo SKL International Co.,Ltd.
Product Type:
FDA Application Number:	part333A
Marketing Category:	OTC MONOGRAPH NOT FINAL
Start Marketing Date:	5/8/2020

No.	Package Code	Package Description
1	74542-012-01	55 mL in 1 BOTTLE (74542-012-01)
2	74542-012-02	100 mL in 1 BOTTLE (74542-012-02)
3	74542-012-03	300 mL in 1 BOTTLE (74542-012-03)
4	74542-012-04	500 mL in 1 BOTTLE (74542-012-04)
5	74542-012-05	980 mL in 1 BOTTLE (74542-012-05)
6	74542-012-06	1000 mL in 1 BOTTLE (74542-012-06)
7	74542-012-07	1300 mL in 1 BOTTLE (74542-012-07)
8	74542-012-08	2000 mL in 1 BOTTLE (74542-012-08)
9	74542-012-09	5000 mL in 1 BOTTLE (74542-012-09)

Field Name	Field Value	Definition
PRODUCT NDC	74542-012	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	PURIDENE	Indicates 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.
START MARKETING DATE	5/8/2020	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAME	OTC MONOGRAPH NOT FINAL	The translation of the dosage form Code submitted by the firm.
APPLICATION NUMBER	part333A	The translation of the route code submitted by the firm, indicating route of administration.
LABELER NAME	Ningbo SKL International Co.,Ltd.	This is the date that the labeler indicates was the start of its marketing of the drug product.