Standard Procedure SPF 50 Sunscreen Face and Body

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBaxter Laboratories

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

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)

Annotations

UNII (FDA Substance ID)

G63QQF2NOX

AVOBENZONE

RxCUI 45045

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "G63QQF2NOX",
    "rxcui": "45045",
    "inchikey": "XNEFYCZVKIDDMS-UHFFFAOYSA-N",
    "display_name": "AVOBENZONE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "34f6150d-9627-94a5-e063-6394a90ad448": {
      "match": "brand_token",
      "title": "STANDARD PROCEDURE SPF 50 SUNSCREEN FACE AND BODY (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [BAXTER LABORATORIES]",
      "spl_version": "2",
      "published_date": "2026-05-20"
    }
  },
  "productid": "70157-027_51babec8-0d7b-9842-e063-6394a90a30fb",
  "productndc": "70157-027",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "Standard Procedure SPF 50 Sunscreen Face and Body",
  "active_ingred_unit": "g/100mL; g/100mL; g/100mL; g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Avobenzone, Homosalate, Octisalate, Octocrylene",
  "start_marketing_date": "20250530",
  "active_numerator_strength": "3; 10; 5; 8"
}

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