KIDS SPF30 SUPER SENSITIVE PLUS C111 SUNSCREEN

UNIISPL

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

Identification

ManufacturerORGANIC & SUSTAINABLE BEAUTY

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5291506829
82 g in 1 TUBE (52915-068-29)

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": {
    "a7ab2140-de09-158f-e053-2a95a90a25a0": {
      "match": "brand_token",
      "title": "KIDS COUGH AND CHEST CONGESTION (DEXTROMETHORPHAN HBR, GUAIFENESIN) SUSPENSION [GENEXA INC.]",
      "spl_version": "12",
      "published_date": "2026-06-01"
    }
  },
  "productid": "52915-068_b198dfe6-503e-48b8-b253-f94c55937a84",
  "productndc": "52915-068",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE",
  "proprietary_name": "KIDS SPF30 SUPER SENSITIVE PLUS C111 SUNSCREEN",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "TITANIUM DIOXIDE",
  "start_marketing_date": "20140203",
  "active_numerator_strength": "120"
}

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