TOPCO TOPCARE EVERYDAY BABY PROTECTION SUN SPF 50

UNIISPL

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

Identification

ManufacturerTOPCO ASSOCIATES LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
3680034711
237 mL in 1 BOTTLE (36800-347-11)

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": {
    "ecf87660-f552-1f6b-e053-2a95a90a2486": {
      "match": "brand_token",
      "title": "TOPCO ASSOCIATES (SELENIUM SULFIDE) SHAMPOO [TOPCO ASSOCIATES]",
      "spl_version": "5",
      "published_date": "2026-05-11"
    }
  },
  "productid": "36800-347_24882f00-521b-2de9-e063-6394a90a1bf9",
  "productndc": "36800-347",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTISALATE; ZINC OXIDE",
  "proprietary_name": "TOPCO TOPCARE EVERYDAY BABY PROTECTION SUN SPF 50",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "OCTISALATE, ZINC OXIDE",
  "start_marketing_date": "20181102",
  "active_numerator_strength": "50; 145"
}

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