KINLO Golden Rays Sunscreen

UNIISPL

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

Identification

ManufacturerA-Frame SunCo Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8218444802
1 BOTTLE, PUMP in 1 CARTON (82184-4480-2) / 50 mL in 1 BOTTLE, PUMP (82184-4480-1)

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": {
    "cb18e5c3-e184-7986-e053-2995a90a5c3b": {
      "match": "brand_token",
      "title": "KINLO GOLDEN RAYS SUNSCREEN (ZINC OXIDE) LOTION [A-FRAME SUNCO INC]",
      "spl_version": "2",
      "published_date": "2025-01-13"
    }
  },
  "productid": "82184-4480_2b4787da-c1fa-234b-e063-6394a90ad479",
  "productndc": "82184-4480",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "KINLO Golden Rays Sunscreen",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20210826",
  "active_numerator_strength": "132"
}

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