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United States · US · US:75936-652_47fcc6e6-af01-b5dc-e063-6294a90ac671
Every. Single. Face. Watery SPF 50
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSupergoop, LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1175936652011.5 mL in 1 PACKET (75936-652-01)
- ndc11759366520210 mL in 1 TUBE (75936-652-02)
- ndc11759366520350 mL in 1 BOTTLE (75936-652-03)
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": {
"d086a9b8-19e5-f713-e053-2995a90aa976": {
"match": "brand_token",
"title": "EVERY. SINGLE. FACE. WATERY SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [SUPERGOOP, LLC]",
"spl_version": "5",
"published_date": "2026-01-14"
}
},
"productid": "75936-652_47fcc6e6-af01-b5dc-e063-6294a90ac671",
"productndc": "75936-652",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "Every. Single. Face. Watery SPF 50",
"active_ingred_unit": "g/100mL; g/100mL; g/100mL; g/100mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Avobenzone, Homosalate, Octisalate, Octocrylene",
"start_marketing_date": "20211111",
"active_numerator_strength": "3; 9; 5; 9"
}Access this data programmatically
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