HEB Face 50 Clear Zinc Sunscreen

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
3780815109
28.4 g in 1 JAR (37808-151-09)

Annotations

UNII (FDA Substance ID)

5A68WGF6WM

OCTOCRYLENE

RxCUI 77674

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "5A68WGF6WM",
    "rxcui": "77674",
    "inchikey": "FMJSMJQBSVNSBF-UHFFFAOYSA-N",
    "display_name": "OCTOCRYLENE",
    "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": "37808-151_248993da-ef19-95dd-e063-6294a90ab936",
  "productndc": "37808-151",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTOCRYLENE; ZINC OXIDE",
  "proprietary_name": "HEB Face 50 Clear Zinc Sunscreen",
  "active_ingred_unit": "mg/g; mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Octocrylene, Zinc Oxide",
  "start_marketing_date": "20200107",
  "active_numerator_strength": "40; 50"
}

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