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United States Β· US Β· US:75936-601_47fc2ce9-2d8c-efda-e063-6294a90a9f5a
Supergoop Glow Screen SPF 40
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSupergoop LLC
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 4
- ndc1175936601021 TUBE in 1 BOX (75936-601-02) / 50 mL in 1 TUBE (75936-601-01)
- ndc11759366010310 mL in 1 TUBE (75936-601-03)
- ndc1175936601041.5 mL in 1 PACKET (75936-601-04)
- ndc1175936601061 TUBE in 1 BOX (75936-601-06) / 20 mL in 1 TUBE (75936-601-05)
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": {
"d2928dd7-a813-4929-e053-2a95a90aaeb4": {
"match": "brand_token",
"title": "SUPERGOOP GLOW SCREEN SPF 40 SHADE 2 GOLDEN HOUR (BROAD SPECTRUM SUNSCREEN) CREAM [SUPERGOOP LLC]",
"spl_version": "6",
"published_date": "2026-01-12"
}
},
"productid": "75936-601_47fc2ce9-2d8c-efda-e063-6294a90a9f5a",
"productndc": "75936-601",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "Supergoop Glow Screen SPF 40",
"active_ingred_unit": "mg/100mL; mg/100mL; mg/100mL; mg/100mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Broad Spectrum Sunscreen",
"start_marketing_date": "20211220",
"active_numerator_strength": "3; 4; 5; 8"
}Access this data programmatically
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