Crunchi Sunlight Daily Facial Sunscreen SPF 30

UNIISPL

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

Identification

ManufacturerCruchi, LLC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7244402000
1 BOTTLE, GLASS in 1 CARTON (72444-0200-0) / 30 mL in 1 BOTTLE, GLASS

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": {
    "4f3bcfa0-e43e-4284-afaa-6488ddd749f0": {
      "match": "brand_token",
      "title": "CRUNCHI SUNLIGHT DAILY FACIAL SUNSCREEN SPF 30 (ZINC OXIDE) LIQUID [CRUCHI, LLC.]",
      "spl_version": "2",
      "published_date": "2025-12-16"
    }
  },
  "productid": "72444-0200_45ff6623-d2bd-8bd1-e063-6394a90a8091",
  "productndc": "72444-0200",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Crunchi Sunlight Daily Facial Sunscreen SPF 30",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20210602",
  "active_numerator_strength": "125"
}

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