Over-the-counter drug · OTC MONOGRAPH DRUG
Yzmoffer Minoxidil Serum (minoxidil serum) NDC 83818-035
Minoxidil 5 g/100mL · Liquid · Topical · Shenzhen Xinxin Yunhai Technology Co., Ltd.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 83818-035-01 | 83818003501 | 2 BOTTLE in 1 BOX (83818-035-01) / 60 mL in 1 BOTTLEMarketed from Jul 6, 2026 |
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)
- Yzmoffer Minoxidil Serum
- Generic name (nonproprietary)
- minoxidil serum
- Active ingredients
- Minoxidil — 5 g/100mL
- Dosage form
- Liquid
- Route
- Topical
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Other FDA classes
- Arteriolar Vasodilation (Physiologic effect)
- Identifiers
- Product ID 83818-035_55ecc699-b913-3e92-e063-6294a90a08a7SPL ID 55ecc699-b913-3e92-e063-6294a90a08a7SPL set ID 55ecc699-b912-3e92-e063-6294a90a08a7RxCUI 311724UNII 5965120SH1
- 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
N483818003501followed by a unit qualifier and the quantityPackage 83818-0035-01. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
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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