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United States· US:69219-103_50c44fa3-d2c0-2939-e063-6394a90af3b5

EXTREME PROTECT SPF 30

A medicinal product containing octinoxate; zinc oxide, registered in United States by SCIENCE OF SKINCARE LLC.

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…normalisedEXTREME PROTECT SPF 30ATC—REGISTER NO.US:69219-103_50c44fa3…PACKS LISTED14CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
OCTINOXATE; ZINC OXIDE
Manufacturer
SCIENCE OF SKINCARE LLC
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 · 14

  • ndc11
    6921910301
    50 g in 1 BOTTLE, PUMP (69219-103-01)
  • ndc11
    6921910302
    1 BOTTLE, PUMP in 1 BOX (69219-103-02) / 50 g in 1 BOTTLE, PUMP (69219-103-01)
  • ndc11
    6921910313
    100 g in 1 BOTTLE, PUMP (69219-103-13)
  • ndc11
    6921910315
    5 g in 1 BOTTLE, PUMP (69219-103-15)
  • ndc11
    6921910328
    240 g in 1 BOTTLE, PUMP (69219-103-28)
  • ndc11
    6921910351
    1 BOTTLE, PUMP in 1 BOX (69219-103-51) / 100 g in 1 BOTTLE, PUMP (69219-103-13)
  • ndc11
    6921910355
    1 BOTTLE, PUMP in 1 BOX (69219-103-55) / 5 g in 1 BOTTLE, PUMP (69219-103-15)
  • ndc11
    69219-103-01
  • ndc11
    69219-103-02
  • ndc11
    69219-103-13
  • ndc11
    69219-103-15
  • ndc11
    69219-103-28
  • ndc11
    69219-103-51
  • ndc11
    69219-103-55

Regulatory notes

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

Same medicine, other countries

Octinoxate; zinc oxide in 1 other country

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

All octinoxate; zinc oxide products

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/eb8d754d-4c20-4d6f-a432-7e9c06eee6bb
GET /v1/drugs/eb8d754d-4c20-4d6f-a432-7e9c06eee6bb?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": "5.5; 4.12",
  "substance": "OCTINOXATE; ZINC OXIDE",
  "productndc": "69219-103",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "strength_unit": "g/100g; g/100g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about octinoxate; zinc oxide.

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.