Odaban Antiperspirant Deo Stick (antiperspirant antisudorifique) NDC 84788-0003

NDC codes

FDA NDC Directory

Product NDC (as listed)84788-0003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width84788-0003Add 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
84788-0003-1	84788000301	62 mL in 1 BOTTLE (84788-0003-1)Marketed from Dec 1, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Odaban Antiperspirant Deo Stick
Generic name (nonproprietary): antiperspirant antisudorifique
Active ingredients: Aluminum chloride — 12.4 mg/62mL
Dosage form: Stick
Route: Topical
Labeler: Ryma-Pharm GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Dec 1, 2025
Listing expires: Dec 31, 2027
Identifiers: Product ID 84788-0003_47a8b336-87ba-eab8-e063-6294a90aa0c0SPL ID 47a8b336-87ba-eab8-e063-6294a90aa0c0SPL set ID 47a8b358-e7b0-e877-e063-6294a90a6e4cUNII 3CYT62D3GAUPC 5025381000123

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

N484788000301 followed by a unit qualifier and the quantity

Package 84788-0003-01. 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 Jan 5, 2026.

Indications (excerpt from the label)

For external use only. Do not use on broken skin. Stop use if rash or irritation occurs. ‘Aska doctor before use if you have kidney disease. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)