SPF 30 Daily Sunscreen

UNIISPL

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

Identification

ManufacturerBrand Evangelists for Beauty Ltd.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8113600101
1 TUBE in 1 CARTON (81136-001-01) / 50 mL 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": {
    "e97d82fe-cd45-43a5-9c1f-3900025240a1": {
      "match": "brand_token",
      "title": "SPF 50 MINERAL SUNSCREEN FACE AND BODY (ZINC OXIDE) LOTION [TODDLE BORN WILD, INC.]",
      "spl_version": "3",
      "published_date": "2026-05-28"
    }
  },
  "productid": "81136-001_1250ff1a-90a4-9d47-e063-6394a90ad3ae",
  "productndc": "81136-001",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "SPF 30 Daily Sunscreen",
  "active_ingred_unit": "mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20210419",
  "active_numerator_strength": "220"
}

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