58766-020 NDC - SNOWBALM ADULT ()

Drug Information

No.	Package Code	Package Description	Billing Unit
1	58766-020-12	57 g in 1 JAR (58766-020-12)

Field Name	Field Value	Definition
PRODUCT NDC	58766-020	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	SnowBalm Adult	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	3/21/2017	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
END MARKETING DATE	9/7/2021	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 FINAL	The translation of the dosage form Code submitted by the firm.
APPLICATION NUMBER	part347	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.
LABELER NAME	Snow Pharmaceuticals, LLC	This is the date that the labeler indicates was the start of its marketing of the drug product.