Sunscreen SPF 50

UNIISPL

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

Identification

ManufacturerGuangzhou Ariel Biotech Co., Ltd.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8414800201
50 g in 1 BOTTLE (84148-002-01)

Annotations

UNII (FDA Substance ID)

4X49Y0596W

OCTISALATE

RxCUI 91327

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4X49Y0596W",
    "rxcui": "91327",
    "inchikey": "FMRHJJZUHUTGKE-UHFFFAOYSA-N",
    "display_name": "OCTISALATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "1cb7fbca-0874-ae53-e063-6294a90ab42a": {
      "match": "brand_token",
      "title": "SUNSCREEN FOR BABY SPF50PLUS (OCTOCRYLENE,ETHYLHEXYL METHOXYCINNAMATE,TITANIUM DIOXIDE,ETHYLHEXYL SALICYLATE) LOTION [GUANGZHOU SENMAI BIOTECHNOLOGY CO., LTD.]",
      "spl_version": "7",
      "published_date": "2026-04-03"
    }
  },
  "productid": "84148-002_4c53a5da-cf97-f8ed-e063-6294a90a46f1",
  "productndc": "84148-002",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTISALATE; OCTOCRYLENE; ZINC OXIDE",
  "proprietary_name": "Sunscreen SPF 50",
  "active_ingred_unit": "g/100g; g/100g; g/100g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Sunscreen SPF 50",
  "start_marketing_date": "20240312",
  "active_numerator_strength": "5; 8; 3"
}

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