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United States Β· US Β· US:37808-998_248a92b6-98ab-748e-e063-6394a90a87bf
H.E.B
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerH.E.B
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 1
- ndc113780899837156 g in 1 CAN (37808-998-37)
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": {
"2e183ba8-1b83-4211-bc08-dbdcee942ce9": {
"match": "brand_token",
"title": "H.E.B SOLUTIONS SUNSCREEN (ULTRA SPF 50 CONTINUOUS SPRAY) AEROSOL, SPRAY [H.E.B]",
"spl_version": "2",
"published_date": "2024-10-18"
}
},
"productid": "37808-998_248a92b6-98ab-748e-e063-6394a90a87bf",
"productndc": "37808-998",
"dosage_form": "AEROSOL, SPRAY",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "H.E.B",
"active_ingred_unit": "mg/g; mg/g; mg/g; mg/g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "SPF 50 Sunscreen",
"start_marketing_date": "20190307",
"active_numerator_strength": "30; 100; 50; 40"
}Access this data programmatically
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