Dr. Perrys Day Thyme SPF 20 Broad Spectrum Sunscreen

UNIISPL

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

Identification

ManufacturerEnglewood Lab, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
1426801700
1 BOTTLE in 1 CARTON (14268-017-00) / 50 mL in 1 BOTTLE

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": {
    "6c5adc3c-9d45-449a-ad42-f9571851cd18": {
      "match": "brand_token",
      "title": "DR. JOHNE SKIN TAG REMOVER (SALICYLIC ACID) SOLUTION [DR.JOHNES LLC]",
      "spl_version": "9",
      "published_date": "2026-05-28"
    }
  },
  "productid": "14268-017_0c5b5d59-a2e3-2550-e063-6394a90aa2bd",
  "productndc": "14268-017",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "Dr. Perrys Day Thyme SPF 20 Broad Spectrum Sunscreen",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20160404",
  "active_numerator_strength": "100"
}

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