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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
- ndc1185421001001 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"
}Access this data programmatically
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