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United States · US · US:85421-001_30f0f6c2-76bd-0442-e063-6294a90a8c61

Suntan

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerGuangzhou shangwei Beauty TechnologyCo.,Ltd.
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    8542100100
    1 BOTTLE, PLASTIC in 1 BOX, UNIT-DOSE (85421-001-00) / 1 CREAM, AUGMENTED in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)
059QF0KO0R
WATER
RxCUI 11295
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "059QF0KO0R",
    "rxcui": "11295",
    "inchikey": "XLYOFNOQVPJJNP-UHFFFAOYSA-N",
    "display_name": "WATER",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "CUTANEOUS",
  "spl_meta": {
    "30f0f6c2-76bc-0442-e063-6294a90a8c61": {
      "match": "brand_token",
      "title": "SUNTAN (SUNTAN LOTION) CREAM, AUGMENTED [GUANGZHOU SHANGWEI BEAUTY TECHNOLOGYCO.,LTD.]",
      "spl_version": "1",
      "published_date": "2025-03-26"
    }
  },
  "productid": "85421-001_30f0f6c2-76bd-0442-e063-6294a90a8c61",
  "productndc": "85421-001",
  "dosage_form": "CREAM, AUGMENTED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "WATER",
  "proprietary_name": "Suntan",
  "active_ingred_unit": "g/1001",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Suntan Lotion",
  "start_marketing_date": "20250322",
  "active_numerator_strength": "50"
}

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