76144-611 NDC - PAULAS CHOICE CLEAR DAILY SKIN CLEARING TREATMENT ()

Drug Information

Product NDC: 76144-611

Proprietary Name: Paulas Choice Clear Daily Skin Clearing Treatment

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Paula's Choice, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/7/2012

Package Information

No. Package Code Package Description Billing Unit
176144-611-0067 mL in 1 TUBE (76144-611-00)
276144-611-0167 mL in 1 TUBE (76144-611-01)
376144-611-0215 mL in 1 TUBE (76144-611-02)
476144-611-032 mL in 1 PACKET (76144-611-03)C112160
576144-611-0715 mL in 1 TUBE (76144-611-07)

NDC Record

Field Name Field Value Definition
PRODUCT NDC76144-611The 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 NAMEPaulas Choice Clear Daily Skin Clearing TreatmentThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/7/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPaula's Choice, LLCName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC76144-611The 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 NAMEPaulas Choice Clear Daily Skin Clearing TreatmentThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/7/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEPaula's ChoiceName 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