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 · 2

ndc11
5906212001
1 APPLICATOR in 1 BLISTER PACK (59062-1200-1) / 13 g in 1 APPLICATOR
ndc11
5906212002
2 APPLICATOR in 1 BLISTER PACK (59062-1200-2) / 13 g in 1 APPLICATOR

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": {
    "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": "59062-1200_d1f4c797-2359-448a-8112-f69f227f475d",
  "productndc": "59062-1200",
  "dosage_form": "STICK",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "SPF 50 plus Sunscreen",
  "active_ingred_unit": "mg/g; mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "TITANIUM DIOXIDE and ZINC OXIDE",
  "start_marketing_date": "20130621",
  "active_numerator_strength": "79; 67"
}

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