Glowscreen SPF 40 - Dawn

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerSupergoop, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
7593660602
1 TUBE in 1 CARTON (75936-606-02) / 50 mL in 1 TUBE (75936-606-01)
ndc11
7593660603
10 mL in 1 TUBE (75936-606-03)

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": {
    "f7e493da-8fc6-191d-e053-6294a90aa483": {
      "match": "brand_token",
      "title": "GLOWSCREEN SPF 40 -SUNSET (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [SUPERGOOP, LLC]",
      "spl_version": "3",
      "published_date": "2026-01-12"
    }
  },
  "productid": "75936-606_47fc2bd8-f929-755c-e063-6394a90ab0e1",
  "productndc": "75936-606",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "Glowscreen SPF 40 - Dawn",
  "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": "20230315",
  "active_numerator_strength": "3; 4; 5; 8"
}

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