PanOxyl Oil AM Control Moisturizer

UNIISPL

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

Identification

ManufacturerCrown Laboratories

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0316026917
1 TUBE in 1 CARTON (0316-0269-17) / 48 g in 1 TUBE

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": {
    "507150a0-9c20-4a2e-e063-6394a90ab9c7": {
      "match": "brand_token",
      "title": "PANOXYL ACNE CLEARING SPOT TREATMENT (BENZOYL PEROXIDE) GEL [CROWN LABORATORIES]",
      "spl_version": "1",
      "published_date": "2026-06-02"
    }
  },
  "productid": "0316-0269_48342b61-8ca5-3117-e063-6294a90ac21a",
  "productndc": "0316-0269",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "PanOxyl Oil AM Control Moisturizer",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20230113",
  "active_numerator_strength": "170"
}

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