HEB Glow 40 Tinted Sunscreen Face Primer

UNIISPL

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

Identification

ManufacturerH.E.B.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
3780815409
89 mL in 1 TUBE (37808-154-09)

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": {
    "b76c3591-6383-4661-b3db-7a56b11202f7": {
      "match": "brand_token",
      "title": "HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB]",
      "spl_version": "15",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37808-154_3146b1ba-c81f-e27d-e063-6394a90af602",
  "productndc": "37808-154",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "HEB Glow 40 Tinted Sunscreen Face Primer",
  "active_ingred_unit": "mg/mL; mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "AVOBENZONE, OCTISALATE, OCTOCRYLENE",
  "start_marketing_date": "20240118",
  "active_numerator_strength": "30; 50; 100"
}

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