Sunceutical SPF 50 Mineral Body 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
7015736802
1 JAR in 1 CARTON (70157-368-02) / 100 mL in 1 JAR (70157-368-01)
ndc11
7015736804
1 CUP in 1 CARTON (70157-368-04) / 100 mL in 1 CUP (70157-368-03)

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": "70157-368_2c28198b-2028-f0d0-e063-6294a90aa05b",
  "productndc": "70157-368",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Sunceutical SPF 50 Mineral Body Cream",
  "active_ingred_unit": "g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20250120",
  "active_numerator_strength": "20"
}

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