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United States · US · US:80489-235_3134c223-e293-e2e6-e063-6294a90a7cfb
Drs. pharmacy sunscreen SPF 50
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerOL PHARMA TECH LLC. (Drs. Pharmacy)
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc118048923501133 g in 1 TUBE (80489-235-01)
- ndc118048923502118 g in 1 TUBE (80489-235-02)
- ndc11804892350385 g in 1 TUBE (80489-235-03)
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": {
"49a73b0f-90d9-3a4b-e063-6294a90acfb0": {
"match": "brand_token",
"title": "DRS. PHARMACY TRIPLE ANTIBIOTIC PLUS LIDOCAINE (BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, LIDOCAINE OINTMENT) OINTMENT [OL PHARMA TECH, LLC]",
"spl_version": "1",
"published_date": "2026-02-02"
}
},
"productid": "80489-235_3134c223-e293-e2e6-e063-6294a90a7cfb",
"productndc": "80489-235",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "Drs. pharmacy sunscreen SPF 50",
"active_ingred_unit": "g/100g; g/100g; g/100g; g/100g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "sunscreen SPF 50",
"start_marketing_date": "20240101",
"active_numerator_strength": "3; 10; 5; 10"
}Access this data programmatically
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