49527-072 NDC - CLINIQUE BROAD SPECTRUM SPF 30 SUNSCREEN BODY WITH SOLAR SMART ()

Drug Information

Product NDC: 49527-072
Proprietary Name: CLINIQUE BROAD SPECTRUM SPF 30 SUNSCREEN BODY WITH SOLAR SMART
Non Proprietary Name:
Active Ingredient(s):
Administration Route(s):
Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	49527-072-01	1 TUBE in 1 CARTON (49527-072-01) / 150 mL in 1 TUBE

Field Name	Field Value	Definition
PRODUCT NDC	49527-072	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	CLINIQUE BROAD SPECTRUM SPF 30 SUNSCREEN BODY WITH SOLAR SMART	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	6/1/2011	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
END MARKETING DATE	11/16/2020	The translation of the dosage form Code submitted by the firm.
MARKETING CATEGORY NAME	OTC MONOGRAPH NOT FINAL	The translation of the route code submitted by the firm, indicating route of administration.
APPLICATION NUMBER	part352	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	CLINIQUE LABORATORIES LLC	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.