NDC Package 70697-805-02 Aquarelle

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:

70697-805-02

Package Description:

24 POUCH in 1 CASE / .375 mg in 1 POUCH

Product Code:

70697-805

Proprietary Name:

Aquarelle

Usage Information:

For hand washing to decrease bacteria on the skin. May be used on face, arms and legs Throughly wipe hands and face as desired.Allow to dry without wiping.Discard wipe in trash receptacle after use. Do not flush

11-Digit NDC Billing Format:

70697080502

NDC to RxNorm Crosswalk:

RxCUI: 2276303 - benzalkonium Cl 0.125 % Medicated Pad
RxCUI: 2276303 - benzalkonium chloride 1.25 MG/ML Medicated Pad
RxCUI: 2276303 - benzalkonium chloride 0.125 % Medicated Wipe
RxCUI: 2276303 - benzalkonium chloride 0.125 % Topical Cloth
RxCUI: 2276303 - benzalkonium chloride 0.125 % Topical Swab

Labeler Name:

Indelpa, S.a De C.v

Sample Package:

FDA Application Number:

part333E

Marketing Category:

OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.

Start Marketing Date:

10-01-2020

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

70697 - Indelpa, S.a De C.v
- 70697-805 - Aquarelle
  - 70697-805-02 - 24 POUCH in 1 CASE / .375 mg in 1 POUCH

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
70697-805-01	30 PACKAGE in 1 CASE / 15 POUCH in 1 PACKAGE / .375 mg in 1 POUCH
70697-805-03	12 POUCH in 1 CASE / .375 mg in 1 POUCH
70697-805-04	24 POUCH in 1 CASE / .375 mg in 1 POUCH
70697-805-05	16 PACKAGE in 1 BOX / 1 POUCH in 1 PACKAGE / .3 mg in 1 POUCH
70697-805-06	24 POUCH in 1 CASE / .375 mg in 1 POUCH

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70697-805-02?

The NDC Packaged Code 70697-805-02 is assigned to a package of 24 pouch in 1 case / .375 mg in 1 pouch of Aquarelle, labeled by Indelpa, S.a De C.v. The product's dosage form is and is administered via form.

Is NDC 70697-805 included in the NDC Directory?

No, Aquarelle with product code 70697-805 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Indelpa, S.a De C.v on October 01, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70697-805-02?

The 11-digit format is 70697080502. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	70697-805-02	5-4-2	70697-0805-02

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