Sunsolve MD Correct and Fade

UNIISPL

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

Identification

ManufacturerSunsolve MD Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8487820002
1 BOTTLE, PUMP in 1 CARTON (84878-200-02) / 48 mL in 1 BOTTLE, PUMP (84878-200-01)

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": {
    "26a54f00-d84d-8fe3-e063-6394a90a03e8": {
      "match": "brand_token",
      "title": "SUNSOLVE MD MINERAL SHADE QUARTZ 001 (ZINC OXIDE) LOTION [SUNSOLVE MD INC]",
      "spl_version": "5",
      "published_date": "2026-05-25"
    }
  },
  "productid": "84878-200_4395a3a6-6fe6-e6b9-e063-6294a90ae938",
  "productndc": "84878-200",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Sunsolve MD Correct and Fade",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20241106",
  "active_numerator_strength": "132"
}

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