11822-4650 NDC - PURE SPRING ()

Drug Information

Product NDC: 11822-4650

Proprietary Name: PURE SPRING

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: RITE AID
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/1/2012

Package Information

No. Package Code Package Description Billing Unit
111822-4650-9260 mL in 1 BOTTLE, PLASTIC (11822-4650-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC11822-4650The 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 NAMEPURE SPRINGThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/1/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERITE AIDName 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