LEBELAGE UV SUN ULTRA SHIELD SUNSTICK

UNIISPL

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

Identification

ManufacturerDONGDONGGURIMOO CO.,LTD.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8594801002
1 BOTTLE, PLASTIC in 1 BOX (85948-010-02) / 20 g in 1 BOTTLE, PLASTIC (85948-010-01)

Annotations

UNII (FDA Substance ID)

G63QQF2NOX

AVOBENZONE

RxCUI 45045

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "G63QQF2NOX",
    "rxcui": "45045",
    "inchikey": "XNEFYCZVKIDDMS-UHFFFAOYSA-N",
    "display_name": "AVOBENZONE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "4907eb9c-3978-27ed-e063-6394a90a9f66": {
      "match": "brand_token",
      "title": "LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50G (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE, OCTISALATE) LOTION [DONGDONGGURIMOO CO.,LTD.]",
      "spl_version": "1",
      "published_date": "2026-01-26"
    }
  },
  "productid": "85948-010_39eea53d-2d43-da1f-e063-6394a90a839e",
  "productndc": "85948-010",
  "dosage_form": "STICK",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "LEBELAGE UV SUN ULTRA SHIELD SUNSTICK",
  "active_ingred_unit": "g/20g; g/20g; g/20g; g/20g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Avobenzone, Homosalate, Octocrylene, Octyl salicylate",
  "start_marketing_date": "20250722",
  "active_numerator_strength": ".6; 2; 1; 2"
}

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