Over-the-counter drug · OTC MONOGRAPH DRUG
QQE Fungal Nail Treatment (Tolnaftate 1%) NDC 87204-161
Tolnaftate .15 mg/15g · Liquid · Topical · Guangzhou Huixue Biotechnology Co., Ltd.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 87204-161-01 | 8720401610187204016101 | 15 g in 1 BOTTLE, PLASTIC (87204-161-01)Marketed from Jan 30, 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)
- QQE Fungal Nail Treatment
- Generic name (nonproprietary)
- tolnaftate 1%
- Active ingredients
- Tolnaftate — .15 mg/15g
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- Guangzhou Huixue Biotechnology Co., Ltd.NDC labeler code 87204
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 029
- Marketing start
- Marketing end
- Identifiers
- Product ID 87204-161_499c0bab-e7c7-9f20-e063-6294a90aae8bSPL ID 499c0bab-e7c7-9f20-e063-6294a90aae8bSPL set ID 499c0bab-e7c6-9f20-e063-6294a90aae8bUNII 06KB629TKV
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
N487204016101followed by a unit qualifier and the quantityPackage 87204-0161-01. 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)
1. Clean the affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. Gently file the nail to make it thinner and remove debris, being cautious not to harm the nail bed. For best results, file nails every 2-3 days. 2. Supervise children in the use of this product. For athlete's foot: Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. To prevent athlete's foot, apply once or twice daily (morning and/or night). For toe fungus, apply to skin around the nail and cuticle. Visible improvement may be seen in as little as 7 days…
Excerpt only. Read the full label for complete information.
About NDC 87204-161
- What is NDC 87204-161?
- 87204-161 is the product NDC for QQE Fungal Nail Treatment (tolnaftate 1%), Tolnaftate .15 mg/15g liquid, listed with the FDA by Guangzhou Huixue Biotechnology Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- QQE Fungal Nail Treatment (Tolnaftate 1%).
- What is the active ingredient?
- Tolnaftate.
- Who is the labeler?
- Guangzhou Huixue Biotechnology Co., Ltd., NDC labeler code 87204. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for QQE Fungal Nail Treatment?
- 1 other product NDC are listed under this name. See all QQE Fungal Nail Treatment NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other QQE Fungal Nail Treatment products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| QQE Fungal Nail Treatmenttolnaftate 1% | Tolnaftate 1 mg/15mL | CreamTopical | Guangzhou Huixue Biotechnology Co., Ltd. | 87204-175 | 87204-0175-01 |
Other NDCs under M 029
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 |
|---|---|---|---|---|
| Aavrani Dry Scalp Rescue Serumsalicylic acid | Salicylic acid 18 mg/mL | LiquidTopical | AAVRANI, INC. | 83707-426 |