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  5. NDC Package Code: 84178-009-03 Kiwi Antiperspirant Deodorant Roll-on

NDC Package 84178-009-03 Kiwi Antiperspirant Deodorant Roll-on

Antiperspirant Deodorant Roll-on Cream Cutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
84178-009-03
Package Description:
80 g in 1 BOTTLE, PLASTIC
Product Code:
84178-009
Proprietary Name:
Kiwi Antiperspirant Deodorant Roll-on
Non-Proprietary Name:
Antiperspirant Deodorant Roll-on
Substance Name:
Aluminum Chlorohydrate
Usage Information:
Do not use on broken skin.Stop use if rash or irritation occurs.
11-Digit NDC Billing Format:
84178000903
Product Type:
Human Otc Drug
Labeler Name:
Evi Labs
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
Cutaneous - Administration to the skin.
Active Ingredient(s):
ALUMINUM CHLOROHYDRATE 8 g/80g
Sample Package:
No
FDA Application Number:
M019
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
01-31-2024
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
Code Structure:

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.

Frequently Asked Questions

What is NDC 84178-009-03?

The NDC Packaged Code 84178-009-03 is assigned to a package of 80 g in 1 bottle, plastic of Kiwi Antiperspirant Deodorant Roll-on, a human over the counter drug labeled by Evi Labs. The product's dosage form is cream and is administered via cutaneous form.

Is NDC 84178-009 included in the NDC Directory?

Yes, Kiwi Antiperspirant Deodorant Roll-on with product code 84178-009 is active and included in the NDC Directory. The product was first marketed by Evi Labs on January 31, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 84178-009-03?

The 11-digit format is 84178000903. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-284178-009-035-4-284178-0009-03