doTERRA sun Face Daily Moisturizer

UNIISPL

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

Identification

ManufacturerdoTERRA International, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7163014715
50 g in 1 BOTTLE, PUMP (71630-147-15)

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": {
    "f3836517-e3ec-5e9e-e053-2a95a90a7af1": {
      "match": "brand_token",
      "title": "DOTERRA SUN FACE DAILY MOISTURIZER (ZINC OXIDE) LOTION [DOTERRA INTERNATIONAL, LLC]",
      "spl_version": "4",
      "published_date": "2025-02-10"
    }
  },
  "productid": "71630-147_2ccc5c4c-bc82-53f1-e063-6394a90a705c",
  "productndc": "71630-147",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "doTERRA sun Face Daily Moisturizer",
  "active_ingred_unit": "g/100g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc oxide",
  "start_marketing_date": "20230501",
  "active_numerator_strength": "13"
}

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