70342-102 NDC - SUN BATHE SUNSCREEN ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	70342-102-13	99 g in 1 PACKAGE (70342-102-13)

Field Name	Field Value	Definition
PRODUCT NDC	70342-102
PROPRIETARY NAME	SUN BATHE SUNSCREEN	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX	SPF 20	This is the date that the labeler indicates was the start of its marketing of the drug product.
START MARKETING DATE	5/23/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	OTC MONOGRAPH 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.
APPLICATION NUMBER	part352	Name of Company corresponding to the labeler code segment of the Product NDC.
LABELER NAME	BABY BUBBA ENTERPRISES INC	Name of Company corresponding to the labeler code segment of the Product NDC.