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United States · US · US:84469-721_3f724e4a-a6d4-f837-e063-6394a90ac084
ESPOIR WATER SPLASH SUN SERUM
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerESPOIR Corporation
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1184469721011 BOTTLE, PUMP in 1 BOX (84469-721-01) / 50 mL in 1 BOTTLE, PUMP
- ndc1184469721032 BOX in 1 BLISTER PACK (84469-721-03) / 1 BOTTLE, PUMP in 1 BOX / 50 mL in 1 BOTTLE, PUMP
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": {
"1c4e7ba2-05e8-f949-e063-6394a90a699d": {
"match": "brand_token",
"title": "ESPOIR WATER SPLASH SUN SERUM (HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE) LOTION [ESPOIR CORPORATION]",
"spl_version": "4",
"published_date": "2025-12-11"
}
},
"productid": "84469-721_3f724e4a-a6d4-f837-e063-6394a90ac084",
"productndc": "84469-721",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "ESPOIR WATER SPLASH SUN SERUM",
"active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "homosalate, octocrylene, octisalate, avobenzone",
"start_marketing_date": "20240902",
"active_numerator_strength": "30; 95; 45; 50"
}Access this data programmatically
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