What is NDC 83004-015?

83004-015 is the product NDC for Medicated Foaming Feminine, Lactic acid .5 g/100mL + 4 more ingredients gel, listed with the FDA by Rida LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Medicated Foaming Feminine (Lactic acid, Boric acid, Chlorhexidine gluconate, Cnidium monnieri fruit, Levomenol).

What is the active ingredient?

Lactic acid, Boric acid, Chlorhexidine gluconate, Cnidium monnieri fruit oil, Levomenol.

Rida LLC, NDC labeler code 83004. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Medicated Foaming Feminine?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Medicated Foaming Feminine NDC 83004-015

NDC codes

FDA NDC Directory

Product NDC (as listed)83004-015Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83004-0015Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
83004-015-01	83004001501	1 BOTTLE in 1 BOX (83004-015-01) / 150 mL in 1 BOTTLEMarketed from Feb 27, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Medicated Foaming Feminine
Generic name (nonproprietary): lactic acid, boric acid, chlorhexidine gluconate, cnidium monnieri fruit, levomenol
Active ingredients: Lactic acid — .5 g/100mLBoric acid — .5 g/100mLChlorhexidine gluconate — 1 g/100mLCnidium monnieri fruit oil — .5 g/100mLLevomenol — .3 g/100mL
Dosage form: Gel
Route: Topical
Labeler: Rida LLCNDC labeler code 83004
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 27, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Decreased Cell Wall Integrity (Physiologic effect)
Identifiers: Product ID 83004-015_2fae9a9c-1b17-5954-e063-6394a90ac2edSPL ID 2fae9a9c-1b17-5954-e063-6394a90ac2edSPL set ID 02b3d683-05b0-4075-bbf9-e6d97c61765cUNII 33X04XA5AT, R57ZHV85D4, MOR84MUD8E, JK0MS9P8YL, 24WE03BX2T

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N483004001501 followed by a unit qualifier and the quantity

Package 83004-0015-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 6, 2025.

Indications (excerpt from the label)

Uses ● Antimicrobial action: Effectively targets and eliminates harmful bacteria to maintain natural balance. ● UTI Defense: Actively helps to prevent urinary tract infections. ● Odor Control: Neutralizes odors, leaving you feeling fresh and clean.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 83004-015

What is NDC 83004-015?: 83004-015 is the product NDC for Medicated Foaming Feminine, Lactic acid .5 g/100mL + 4 more ingredients gel, listed with the FDA by Rida LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Medicated Foaming Feminine (Lactic acid, Boric acid, Chlorhexidine gluconate, Cnidium monnieri fruit, Levomenol).
What is the active ingredient?: Lactic acid, Boric acid, Chlorhexidine gluconate, Cnidium monnieri fruit oil, Levomenol.
Who is the labeler?: Rida LLC, NDC labeler code 83004. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Medicated Foaming Feminine?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.