79996-100 NDC - AQUA GEL ADVANCED FORMULA ()

Drug Information

Product NDC: 79996-100

Proprietary Name: Aqua Gel advanced formula

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: EPOXEMEX, S.A. DE C.V.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/30/2020

Package Information

No. Package Code Package Description Billing Unit
179996-100-0152 mL in 1 BOTTLE, PLASTIC (79996-100-01)
279996-100-02170 mL in 1 BOTTLE, PLASTIC (79996-100-02)
379996-100-031000 mL in 1 BOTTLE, PLASTIC (79996-100-03)
479996-100-044000 mL in 1 TANK (79996-100-04)

NDC Record

Field Name Field Value Definition
PRODUCT NDC79996-100The 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 NAMEAqua Gel advanced formulaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/30/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEEPOXEMEX, S.A. DE C.V.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