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United States· US:70108-324_f68d5aff-15ee-40f8-93fb-658d53875140

Smart Care OCEAN BREEZE HAND SANITIZER

A medicinal product containing alcohol, registered in United States by Ashtel Studios, Inc..

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedSmart Care OCEAN BREEZE HAND SANITIZERATC—REGISTER NO.US:70108-324_f68d5aff…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ALCOHOL
Manufacturer
Ashtel Studios, 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 · 2

  • ndc11
    7010832401
    1 BOTTLE, SPRAY in 1 POUCH (70108-324-01) / 30 mL in 1 BOTTLE, SPRAY
  • ndc11
    70108-324-01

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Alcohol in 9 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All alcohol products

Authorised across Europe · EMA

The same active substance is authorised in 10 EEA countries. Names it is sold under:

  • Belgium · Ethanol 96° Sterop
  • Bulgaria · Етилов Спирт, Етилов Спирт Bt
  • Germany · Ahd 2000, Alkohol-Konzentrat Braun
  • Spain · Alcohol Sanitario Reig Jofre
  • France · Alcool Modifie, Alcool Modifié Gifrer
  • Greece · Οινοπνευμα Mediplants, Οινοπνευμα Φαρμακευτικο Mediplants
  • Hungary · Alkohol Pharmamagist
  • Luxembourg · Alkohol-Konzentrat Braun, Sterillium Med
  • Poland · Desderman, Gargarisma Prophylacticum
  • Slovakia · Spiritus Concentratus Vulm, Spiritus Dilutus Vulm

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/aaf63700-819e-478b-aca0-54fc7579e66a
GET /v1/drugs/aaf63700-819e-478b-aca0-54fc7579e66a?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": "70",
  "substance": "ALCOHOL",
  "productndc": "70108-324",
  "dosage_form": "SPRAY",
  "dea_schedule": null,
  "strength_unit": "mL/100mL",
  "application_number": "505G(a)(3)",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about alcohol.

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.