69176-070 NDC - RAPID GEL RX ()

Drug Information

Product NDC: 69176-070

Proprietary Name: Rapid Gel Rx

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: TMIG Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/20/2016

Package Information

No. Package Code Package Description Billing Unit
169176-070-301 TUBE in 1 CARTON (69176-070-30) / 30 mL in 1 TUBEGM
269176-070-901 TUBE in 1 CARTON (69176-070-90) / 90 mL in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC69176-070The 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 NAMERapid Gel RxThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/20/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETMIG IncName 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