Over-the-counter drug · ANDA
Foligain Professional Series Extra Strength for Women Minoxidil Topical Hair Regrowth Treatment (Minoxidil) NDC 69607-9530
Minoxidil 20 mg/mL · Solution · Topical · WR Group, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 69607-9530-0 | 6960795300069607953000 | 3 BOTTLE, DROPPER in 1 BOX (69607-9530-0) / 60 mL in 1 BOTTLE, DROPPERMarketed from May 5, 2026 |
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)
- Foligain Professional Series Extra Strength for Women Minoxidil Topical Hair Regrowth Treatment
- Generic name (nonproprietary)
- minoxidil
- Active ingredients
- Minoxidil — 20 mg/mL
- Dosage form
- Solution
- Route
- Topical
- Labeler
- WR Group, Inc.NDC labeler code 69607
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 078176
- Marketing start
- Listing expires
- Other FDA classes
- Arteriolar Vasodilation (Physiologic effect)
- Identifiers
- Product ID 69607-9530_51b0803c-0bbd-c834-e063-6294a90aab95SPL ID 51b0803c-0bbd-c834-e063-6294a90aab95SPL set ID a765cc59-ab59-4e49-ba28-926a2e0a78b1RxCUI 311723UNII 5965120SH1UPC 0850080512050
- Pharmacologic class
- 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
N469607953000followed by a unit qualifier and the quantityPackage 69607-9530-00. 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)
Use to regrow hair on the scalp. (see picture on side of carton)
Excerpt only. Read the full label for complete information.
About NDC 69607-9530
- What is NDC 69607-9530?
- 69607-9530 is the product NDC for Foligain Professional Series Extra Strength for Women Minoxidil Topical Hair Regrowth Treatment, Minoxidil 20 mg/mL solution, listed with the FDA by WR Group, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Foligain Professional Series Extra Strength for Women Minoxidil Topical Hair Regrowth Treatment (Minoxidil).
- What is the active ingredient?
- Minoxidil.
- Who is the labeler?
- WR Group, Inc., NDC labeler code 69607. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Foligain Professional Series Extra Strength for Women Minoxidil Topical Hair Regrowth Treatment?
- 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 ANDA 078176
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.