SPF 50 plus Sunscreen

UNIISPL

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

Identification

ManufacturerKAS Direct LLC dba BabyGanics

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5906210008
236 mL in 1 TUBE (59062-1000-8)

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": {
    "e97d82fe-cd45-43a5-9c1f-3900025240a1": {
      "match": "brand_token",
      "title": "SPF 50 MINERAL SUNSCREEN FACE AND BODY (ZINC OXIDE) LOTION [TODDLE BORN WILD, INC.]",
      "spl_version": "3",
      "published_date": "2026-05-28"
    }
  },
  "productid": "59062-1000_a7636b53-d9d4-4c4f-929a-515a8cc78659",
  "productndc": "59062-1000",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "SPF 50 plus Sunscreen",
  "active_ingred_unit": "mg/mL; mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Titanium Dioxide, OCTISALATE, and ZINC OXIDE",
  "start_marketing_date": "20170724",
  "active_numerator_strength": "50; 30; 60"
}

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