Sunscreen

UNIISPLATC D02BA02

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

Identification

ManufacturerMAIDORA CO.,LTD

CountryUS (United States)

ATC codeD02BA02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8724312335
5 CANISTER in 1 BOX (87243-123-35) / 1 CREAM in 1 CANISTER

Annotations

UNII (FDA Substance ID)

4Y5P7MUD51

OCTINOXATE

RxCUI 13369

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4Y5P7MUD51",
    "rxcui": "13369",
    "inchikey": "YBGZDTIWKVFICR-JLHYYAGUSA-N",
    "display_name": "OCTINOXATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS",
  "spl_meta": {
    "1cb7fbca-0874-ae53-e063-6294a90ab42a": {
      "match": "brand_token",
      "title": "SUNSCREEN FOR BABY SPF50PLUS (OCTOCRYLENE,ETHYLHEXYL METHOXYCINNAMATE,TITANIUM DIOXIDE,ETHYLHEXYL SALICYLATE) LOTION [GUANGZHOU SENMAI BIOTECHNOLOGY CO., LTD.]",
      "spl_version": "7",
      "published_date": "2026-04-03"
    }
  },
  "productid": "87243-123_44136f78-878a-8185-e063-6394a90ad848",
  "productndc": "87243-123",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTINOXATE",
  "proprietary_name": "Sunscreen",
  "active_ingred_unit": "g/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Japanese Sunscreen SPF 50 Super Water Gel Sunscreen 4.22floz(125g) Refill",
  "start_marketing_date": "20251121",
  "active_numerator_strength": "1"
}

Related drugs

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