55926-0012 NDC - SERENITY REMEDY NO. 12 ()

Drug Information

Product NDC: 55926-0012

Proprietary Name: Serenity Remedy No. 12

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Speer Laboratories, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/17/2013

Package Information

No. Package Code Package Description Billing Unit
155926-0012-259 mL in 1 BOTTLE, SPRAY (55926-0012-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55926-0012The 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 NAMESerenity Remedy No. 12The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/17/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESpeer Laboratories, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023