Over-the-counter drug · OTC MONOGRAPH DRUG
Johnson Foam Pro (Finasteride foam with 5% minoxidil) NDC 84539-002
Finasteride .25 g/100g; Minoxidil 5 g/100g · Aerosol, Foam · Topical · JOHNSON BIOPHARMACEUTICAL INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 84539-002-01 | 8453900020184539000201 | 90 g in 1 BOTTLE (84539-002-01)Marketed from Nov 21, 2024 |
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)
- Johnson Foam Pro
- Generic name (nonproprietary)
- finasteride foam with 5% minoxidil
- Active ingredients
- Finasteride — .25 g/100gMinoxidil — 5 g/100g
- Dosage form
- Aerosol, Foam
- Route
- Topical
- Labeler
- JOHNSON BIOPHARMACEUTICAL INC.NDC labeler code 84539
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Other FDA classes
- 5-alpha Reductase Inhibitors (Mechanism)Arteriolar Vasodilation (Physiologic effect)
- Identifiers
- Product ID 84539-002_581d631c-ecc9-940c-e063-6294a90aa0e1SPL ID 581d631c-ecc9-940c-e063-6294a90aa0e1SPL set ID 27697b1c-f713-f7e0-e063-6394a90a7514UNII 57GNO57U7G, 5965120SH1
- Pharmacologic class
- 5-alpha Reductase Inhibitor; Arteriolar Vasodilator
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
N484539000201followed by a unit qualifier and the quantityPackage 84539-0002-01. 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 .
Indications (excerpt from the label)
Fight primarycause ofhalr loss in men.Antihalrlosstohelpincreasehairdenslty andvolume.
Excerpt only. Read the full label for complete information.
About NDC 84539-002
- What is NDC 84539-002?
- 84539-002 is the product NDC for Johnson Foam Pro (finasteride foam with 5% minoxidil), Finasteride .25 g/100g; Minoxidil 5 g/100g aerosol, foam, listed with the FDA by JOHNSON BIOPHARMACEUTICAL INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Johnson Foam Pro (Finasteride foam with 5% minoxidil).
- What is the active ingredient?
- Finasteride, Minoxidil.
- Who is the labeler?
- JOHNSON BIOPHARMACEUTICAL INC., NDC labeler code 84539. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Johnson Foam Pro?
- 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.
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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