HEB Sensitive 50 Mineral Sensitive Skin Sunscreen For Face

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
3780835009
89 mL in 1 TUBE (37808-350-09)

Annotations

UNII (FDA Substance ID)

SOI2LOH54Z

ZINC OXIDE

RxCUI 11423

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "SOI2LOH54Z",
    "rxcui": "11423",
    "inchikey": "RNWHGQJWIACOKP-UHFFFAOYSA-N",
    "display_name": "ZINC OXIDE",
    "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": "37808-350_2489cda6-c2f2-a801-e063-6394a90af088",
  "productndc": "37808-350",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "HEB Sensitive 50 Mineral Sensitive Skin Sunscreen For Face",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20210128",
  "active_numerator_strength": "216"
}

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