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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

  • ndc11
    7593660102
    1 TUBE in 1 BOX (75936-601-02) / 50 mL in 1 TUBE (75936-601-01)
  • ndc11
    7593660103
    10 mL in 1 TUBE (75936-601-03)
  • ndc11
    7593660104
    1.5 mL in 1 PACKET (75936-601-04)
  • ndc11
    7593660106
    1 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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Supergoop Glow Screen SPF 40 (US) β€” Drug Database