Sunceutical SPF 50 Mineral Face Cream

UNIISPL

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

Identification

ManufacturerBaxter Laboratories Pty. Ltd.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
7015736902
1 JAR in 1 CARTON (70157-369-02) / 50 mL in 1 JAR (70157-369-01)
ndc11
7015736904
1 CUP in 1 CARTON (70157-369-04) / 50 mL in 1 CUP (70157-369-03)

Annotations

UNII (FDA Substance ID)

SOI2LOH54Z

ZINC OXIDE

RxCUI 11423

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "SOI2LOH54Z",
    "rxcui": "11423",
    "inchikey": "RNWHGQJWIACOKP-UHFFFAOYSA-N",
    "display_name": "ZINC OXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "2c28198b-2027-f0d0-e063-6294a90aa05b": {
      "match": "brand_token",
      "title": "SUNCEUTICAL SPF 50 MINERAL BODY CREAM (ZINC OXIDE) CREAM [BAXTER LABORATORIES PTY. LTD.]",
      "spl_version": "1",
      "published_date": "2025-01-27"
    }
  },
  "productid": "70157-369_2c408728-a1df-d51e-e063-6294a90ade0b",
  "productndc": "70157-369",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Sunceutical SPF 50 Mineral Face Cream",
  "active_ingred_unit": "g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20250121",
  "active_numerator_strength": "20"
}

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