celimax PORE SKIN CLARIFYING DAILY SUNSCREEN

UNIISPL

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

Identification

ManufacturerABSORBLAB Co., Ltd

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8722615002
1 TUBE in 1 BOX (87226-150-02) / 50 mL in 1 TUBE (87226-150-01)

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": {
    "4edac8d8-523f-8b8b-e063-6294a90a1a25": {
      "match": "brand_token",
      "title": "CELIMAX PORE SKIN CLARIFYING DAILY SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) CREAM [ABSORBLAB CO., LTD]",
      "spl_version": "2",
      "published_date": "2026-04-09"
    }
  },
  "productid": "87226-150_4eec1cff-701d-5667-e063-6294a90a9be1",
  "productndc": "87226-150",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "celimax PORE SKIN CLARIFYING DAILY SUNSCREEN",
  "active_ingred_unit": "g/50mL; g/50mL; g/50mL; g/50mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE",
  "start_marketing_date": "20260407",
  "active_numerator_strength": "1.4; 6.8; 2.3; 4.5"
}

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