NDC Package 83004-015-01 Medicated Foaming Feminine

Lactic Acid,Boric Acid,Chlorhexidine Gluconate,Cnidium Monnieri Fruit,Levomenol Gel - View Billable Units, 11-Digit Format, RxNorm

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:
83004-015-01
Package Description:
1 BOTTLE in 1 BOX / 150 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Medicated Foaming Feminine
Non-Proprietary Name:
Lactic Acid, Boric Acid, Chlorhexidine Gluconate, Cnidium Monnieri Fruit, Levomenol
Substance Name:
Boric Acid; Chlorhexidine Gluconate; Cnidium Monnieri Fruit Oil; Lactic Acid; Levomenol
Usage Information:
● Wet the area: Begin by splashing water on the external vaginal area or take this step while in the shower or bath to ensure the area is moist. ● Apply the wash: Pump a small amount of the foam onto your hand. The foam should be rich and airy. Typically, two pumps are sufficient. ● Gentle Cleansing: Gently apply foam to the delicate areas. Use your hand to spread the foam, covering the entire area with gentle, circular motions. Avoid using sponges or washcloths, as they can be too abrasive. ● Rinse thoroughly: After cleansing, rinse thoroughly with warm water. Ensure all traces of the wash are removed to avoid irritation. ● Pat dry: Gently pat the area with a clean towel. Avoid rubbing, as this may cause irritation. It's important to ensure the area is completely dry before dressing to prevent moisture buildup, which can lead to irritation or infections.
11-Digit NDC Billing Format:
83004001501
Product Type:
Human Otc Drug
Labeler Name:
Rida Llc
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route(s):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
02-27-2025
Listing Expiration Date:
12-31-2026
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.

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Frequently Asked Questions

What is NDC 83004-015-01?

The NDC Packaged Code 83004-015-01 is assigned to a package of 1 bottle in 1 box / 150 ml in 1 bottle of Medicated Foaming Feminine, a human over the counter drug labeled by Rida Llc. The product's dosage form is gel and is administered via topical form.

Is NDC 83004-015 included in the NDC Directory?

Yes, Medicated Foaming Feminine with product code 83004-015 is active and included in the NDC Directory. The product was first marketed by Rida Llc on February 27, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 83004-015-01?

The 11-digit format is 83004001501. 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
5-3-283004-015-015-4-283004-0015-01