68828-500 NDC - JAFRA ROYAL JELLY REVITALIZE ()

Drug Information

Product NDC: 68828-500

Proprietary Name: Jafra Royal Jelly Revitalize

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	JAFRA COSMETICS INTERNATIONAL
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	4/27/2018

No.	Package Code	Package Description	Billing Unit
1	68828-500-01	1 KIT in 1 PACKAGE (68828-500-01) * 7.5 mL in 1 PACKAGE (68828-501-02) * 7.5 mL in 1 PACKAGE * 7.5 mL in 1 TUBE * 7.5 mL in 1 PACKAGE * 14 mL in 1 TUBE * 30 mL in 1 TUBE * 14 mL in 1 TUBE (68828-501-01)

Field Name	Field Value	Definition
PRODUCT NDC	68828-500	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	Jafra Royal Jelly Revitalize	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	4/27/2018	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	JAFRA COSMETICS INTERNATIONAL	Name 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