United States· US:82046-620_53ff6a6c-255b-b052-e063-6394a90ac688
CeraVe Developed with Dermatologists Itch Relief Moisturizing
A medicinal product containing pramoxine hydrochloride, registered in United States by L'Oreal USA Products Inc.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- PRAMOXINE HYDROCHLORIDE
- Manufacturer
- L'Oreal USA Products Inc
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 3
- ndc1182046-620-01
- ndc1182046-620-02
- ndc1182046-620-03
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Pramoxine hydrochloride in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FranceCEMAUKOR 1%, gel pour application localeBOUCHARA-RECORDATI
- CanadaITCH RELIEF MOISTURIZING CREAMCERAVE CANADA
- United KingdomAnugesic-HC suppositoriesPfizer Ltd
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- France · Cemaukor, Pramocaine Chlorhydrate Arrow Conseil
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/d1155798-6eb3-4298-8cfa-af511292fa01 GET /v1/drugs/d1155798-6eb3-4298-8cfa-af511292fa01?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": "10",
"substance": "PRAMOXINE HYDROCHLORIDE",
"productndc": "82046-620",
"dosage_form": "CREAM",
"dea_schedule": null,
"strength_unit": "mg/g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about pramoxine hydrochloride.
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.