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United States · US · US:69949-010_3dc666fa-dd86-4924-9b90-50d240203981

NATURAL MOISTURIZING FACE SUNSCREEN and PRIMER

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerSynchronicity Spa, Inc. DBA Suntegrity
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    6994901001
    50 g in 1 CANISTER (69949-010-01)
  • ndc11
    6994901002
    50 g in 1 BOX (69949-010-02)

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": {
    "49a2430e-c15b-4610-e063-6294a90ac520": {
      "match": "brand_token",
      "title": "NATURAL SENSE SPF 50 SUNSCREEN (SUNSCREEN) CLOTH [DR. NATURAL LLC]",
      "spl_version": "2",
      "published_date": "2026-05-20"
    }
  },
  "productid": "69949-010_3dc666fa-dd86-4924-9b90-50d240203981",
  "productndc": "69949-010",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "NATURAL MOISTURIZING FACE SUNSCREEN and PRIMER",
  "active_ingred_unit": "mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20100812",
  "active_numerator_strength": "200"
}

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