United States· US:59316-835_485c8fe8-339a-6559-e063-6394a90ae8ea
Biofreeze
A menthol product containing menthol, registered in United States by RB Health (US) LLC. The same ATC class is registered in 2 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Menthol is registered in 2 of 19 countries.
Countries holding a registration under ATC R01AX23 (menthol), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 1 of them publish a price we can compare per daily dose
Menthol · ATC R01AX23
2 / 19 countries
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- MENTHOL
- Manufacturer
- RB Health (US) LLC
- Country
- United States (US)
- ATC code
- R01AX23
- ATC class
- Menthol
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- July 12, 2026
Packs & prices · 2
- ndc115931683520118 mL in 1 BOTTLE (59316-835-20)
- ndc1159316-835-20
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Menthol in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomAAA Menthol 1% in Aqueous creamTriOn Pharma Ltd
- BelgiumAlgis-SprayLaboratoria Qualiphar
- SpainVASELINA MENTOLADA ORRAVAN 20 mg/g POMADALaboratorio Reig Jofre, S.A.
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Spain · Vaselina Mentolada Orravan
- Italy · Mentolo Sella
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/c63448b6-8c1b-4d6b-9f17-6d1b95f303c7 GET /v1/drugs/c63448b6-8c1b-4d6b-9f17-6d1b95f303c7?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"route": "TOPICAL",
"source": "ndc",
"strength": "130",
"substance": "MENTHOL",
"productndc": "59316-835",
"dosage_form": "SPRAY",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about menthol.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.