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United States· US:70157-027_51babec8-0d7b-9842-e063-6394a90a30fb

Standard Procedure SPF 50 Sunscreen Face and Body

A medicinal product containing avobenzone; octisalate; homosalate; octocrylene, registered in United States by Baxter Laboratories.

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…normalisedStandard Procedure SPF 50 Sunscreen F…ATC—REGISTER NO.US:70157-027_51babec8…PACKS LISTED10CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
AVOBENZONE; OCTISALATE; HOMOSALATE; OCTOCRYLENE
Manufacturer
Baxter Laboratories
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 · 10

  • ndc11
    7015702701
    60 mL in 1 BOTTLE, PLASTIC (70157-027-01)
  • ndc11
    7015702702
    100 mL in 1 BOTTLE, PLASTIC (70157-027-02)
  • ndc11
    7015702703
    250 mL in 1 BOTTLE, PLASTIC (70157-027-03)
  • ndc11
    7015702704
    500 mL in 1 BOTTLE, PUMP (70157-027-04)
  • ndc11
    7015702705
    35 mL in 1 TUBE (70157-027-05)
  • ndc11
    70157-027-04
  • ndc11
    70157-027-05
  • ndc11
    70157-027-01
  • ndc11
    70157-027-02
  • ndc11
    70157-027-03

Regulatory notes

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

Same medicine, other countries

Avobenzone; octisalate; homosalate; octocrylene in 1 other country

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

All avobenzone; octisalate; homosalate; octocrylene 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/5dca4bb8-e4ca-43b5-8a70-6bab71fc7841
GET /v1/drugs/5dca4bb8-e4ca-43b5-8a70-6bab71fc7841?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": "3; 5; 10; 8",
  "substance": "AVOBENZONE; OCTISALATE; HOMOSALATE; OCTOCRYLENE",
  "productndc": "70157-027",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "strength_unit": "g/100mL; g/100mL; g/100mL; g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about avobenzone; octisalate; homosalate; octocrylene.

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.