HEIMISH RX HYALURONIC ACID HYDRATING SUNSCREEN

UNIISPL

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

Identification

ManufacturerONEAND CO., LTD.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8531500102
1 TUBE in 1 PACKAGE (85315-001-02) / 50 mL in 1 TUBE (85315-001-01)

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": {
    "2dc41560-f4a7-5f0b-e063-6294a90a0630": {
      "match": "brand_token",
      "title": "HEIMISH RX HYALURONIC ACID HYDRATING SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [ONEAND CO., LTD.]",
      "spl_version": "4",
      "published_date": "2025-11-17"
    }
  },
  "productid": "85315-001_43772221-dada-a279-e063-6394a90a39d1",
  "productndc": "85315-001",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "HEIMISH RX HYALURONIC ACID HYDRATING SUNSCREEN",
  "active_ingred_unit": "g/50mL; g/50mL; g/50mL; g/50mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Avobenzone, Homosalate, Octisalate, Octocrylene",
  "start_marketing_date": "20250314",
  "active_numerator_strength": "1.5; 4.5; 2.25; 2.5"
}

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