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United States · US · US:84425-101_4862fbef-e8ad-cc4b-e063-6394a90a35f2
Standard Procedure SPF 50 Sunscreen
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerStandard Procedure Inc
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11844251010160 mL in 1 BOTTLE, PLASTIC (84425-101-01)
- ndc118442510103250 mL in 1 BOTTLE, PLASTIC (84425-101-03)
- ndc118442510104500 mL in 1 BOTTLE, PLASTIC (84425-101-04)
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": {
"34f6150d-9627-94a5-e063-6394a90ad448": {
"match": "brand_token",
"title": "STANDARD PROCEDURE SPF 50 SUNSCREEN FACE AND BODY (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [BAXTER LABORATORIES]",
"spl_version": "2",
"published_date": "2026-05-20"
}
},
"productid": "84425-101_4862fbef-e8ad-cc4b-e063-6394a90a35f2",
"productndc": "84425-101",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "Standard Procedure SPF 50 Sunscreen",
"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": "20240715",
"active_numerator_strength": "30; 100; 50; 80"
}Access this data programmatically
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