Sunscreen

UNIISPL

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

Identification

ManufacturerBaxter of California, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8420300101
30 mL in 1 TUBE (84203-001-01)

Annotations

UNII (FDA Substance ID)

15FIX9V2JP

TITANIUM DIOXIDE

RxCUI 38323

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "15FIX9V2JP",
    "rxcui": "38323",
    "inchikey": "SOQBVABWOPYFQZ-UHFFFAOYSA-N",
    "display_name": "TITANIUM DIOXIDE",
    "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": "84203-001_3aaee79a-2b7f-1b14-e063-6294a90af5b1",
  "productndc": "84203-001",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE",
  "proprietary_name": "Sunscreen",
  "active_ingred_unit": "g/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Titanium Dioxide 6.8%",
  "start_marketing_date": "20240325",
  "active_numerator_strength": ".068"
}

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