69261-007 NDC - QUIP ANTICAVITY ()

Drug Information

Product NDC: 69261-007

Proprietary Name: Quip Anticavity

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Quip NYC Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/25/2021

Package Information

No. Package Code Package Description Billing Unit
169261-007-011 TUBE in 1 CARTON (69261-007-01) / 133 g in 1 TUBE
269261-007-06133 g in 1 TUBE (69261-007-06)
369261-007-07130 g in 1 TUBE (69261-007-07)
469261-007-081 TUBE in 1 CARTON (69261-007-08) / 130 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC69261-007The 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 NAMEQuip AnticavityThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/25/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEQuip NYC Inc.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