Over-the-counter drug · OTC MONOGRAPH DRUG
Menthol Pain Relieving Gel (pain relieving gel) NDC 13709-357
Menthol 4.54 g/227g · Gel · Topical · NeilMed Pharmaceuticals Inc
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 13709-357-01 | 13709035701 | 1 TUBE in 1 CARTON (13709-357-01) / 227 g in 1 TUBEMarketed from May 7, 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)
- Menthol Pain Relieving Gel
- Generic name (nonproprietary)
- pain relieving gel
- Active ingredients
- Menthol — 4.54 g/227g
- Dosage form
- Gel
- Route
- Topical
- Labeler
- NeilMed Pharmaceuticals Inc
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 014
- Marketing start
- Listing expires
- Identifiers
- Product ID 13709-357_513a206c-bbf7-3e51-e063-6294a90adf7aSPL ID 513a206c-bbf7-3e51-e063-6294a90adf7aSPL set ID 513a206c-bbf6-3e51-e063-6294a90adf7aRxCUI 311502UNII L7T10EIP3A
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
N413709035701followed by a unit qualifier and the quantityPackage 13709-0357-01. 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)
Indications Cooling, Pain relieving gel for muscle aches arthiritis pain simple backache Indications
Excerpt only. Read the full label for complete information.
Other NDCs under M 014
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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