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United States · US · US:83542-410_09764ab9-1a62-b42b-e063-6394a90a4a77
JESS BEAUTY Let It Sun Sunscreen SPF-50
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerJESS BEAUTY PRODUCTS LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1183542410001 TUBE in 1 BOX (83542-410-00) / 50 mL in 1 TUBE
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": {
"88628c11-dbc7-4404-9701-7944a685a13d": {
"match": "brand_token",
"title": "JESS BEAUTY LET IT SUN SUNSCREEN SPF-50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [JESS BEAUTY PRODUCTS LLC]",
"spl_version": "2",
"published_date": "2023-11-06"
}
},
"productid": "83542-410_09764ab9-1a62-b42b-e063-6394a90a4a77",
"productndc": "83542-410",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "JESS BEAUTY Let It Sun Sunscreen SPF-50",
"active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE",
"start_marketing_date": "20230630",
"active_numerator_strength": "30; 100; 50; 100"
}Access this data programmatically
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