Over-the-counter drug · ANDA
Minoxidil For Women (Minoxidil) NDC 69113-502
Minoxidil 50 mg/g · Aerosol, Foam · Topical · BosleyMD
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 69113-502-01 | 6911305020169113050201 | 1 CAN in 1 PACKAGE (69113-502-01) / 60 g in 1 CANMarketed from Aug 29, 2025 | |
| 69113-502-02 | 6911305020269113050202 | 2 CAN in 1 PACKAGE (69113-502-02) / 60 g in 1 CANMarketed from Aug 29, 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)
- Minoxidil For Women
- Generic name (nonproprietary)
- minoxidil
- Active ingredients
- Minoxidil — 50 mg/g
- Dosage form
- Aerosol, Foam
- Route
- Topical
- Labeler
- BosleyMDNDC labeler code 69113
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 208092
- Marketing start
- Listing expires
- Other FDA classes
- Arteriolar Vasodilation (Physiologic effect)
- Identifiers
- Product ID 69113-502_0e642b3c-98d8-4262-befb-f7df47661ca8SPL ID 0e642b3c-98d8-4262-befb-f7df47661ca8SPL set ID ebda6e49-140c-4ab0-b155-5ed501ef3e8aRxCUI 645146UNII 5965120SH1UPC 0815266013219
- 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
N469113050201followed by a unit qualifier and the quantityPackage 69113-0502-01. 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)
Use to regrow hair on the top of the scalp (see pictures on side of this carton)
Excerpt only. Read the full label for complete information.
About NDC 69113-502
- What is NDC 69113-502?
- 69113-502 is the product NDC for Minoxidil For Women (minoxidil), Minoxidil 50 mg/g aerosol, foam, listed with the FDA by BosleyMD. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Minoxidil For Women (Minoxidil).
- What is the active ingredient?
- Minoxidil.
- Who is the labeler?
- BosleyMD, NDC labeler code 69113. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Minoxidil For Women?
- 9 other product NDCs are listed under this name. See all Minoxidil For Women NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Minoxidil For Women products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Minoxidil For Womenminoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | CARDINAL HEALTH 110, LLC. DBA LEADER | 70000-0753 | 70000-0753-01 |
| Minoxidil (For Women)minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | Kroger Company | 59450-211 | 59450-0211-02 |
| Minoxidil (For Women)minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | SPAZI INC. | 82376-6007 | 82376-6007-02 |
| Minoxidil (For Women)minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | Walgreen Company | 0363-9091 | 00363-9091-0100363-9091-03 |
| Minoxidil (For Women)minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | TARGET Corporation | 11673-158 | 11673-0158-0411673-0158-08 |
| Minoxidil (For Women)minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | CVS Pharmacy | 51316-213 | 51316-0213-0251316-0213-10 |
| Minoxidil (for Women)minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | SCIENTIFIC HAIR RESEARCH, LLC | 69113-129 | 69113-0129-0169113-0129-02 |
| Minoxidil (for Women)minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | Virtue Labs, LLC | 80855-201 | 80855-0201-0580855-0201-06 |
| Minoxidil For Womenminoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | Sun Pharmaceutical Industries, Inc. | 51672-2129 | 51672-2129-0451672-2129-08 |
Other NDCs under ANDA 208092
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | P & L Development, LLC | 59726-115 |
| Minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | P & L Development, LLC | 59726-116 |
| Minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | P & L Development, LLC | 59726-122 |
| Minoxidil | Minoxidil 50 mg/mL | Aerosol, FoamTopical | P & L Development, LLC | 59726-125 |
| Minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | P & L Development, LLC | 59726-151 |
| Minoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | Keranique | 70550-116 |
| Minoxidil For Menminoxidil | Minoxidil 50 mg/g | Aerosol, FoamTopical | BosleyMD | 69113-501 |