SkinPerfect Primer

UNIISPL

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

Identification

ManufacturerDermalogica, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
6847913000
2 mL in 1 POUCH (68479-130-00)
ndc11
6847913002
1 TUBE in 1 CARTON (68479-130-02) / 22 mL in 1 TUBE
ndc11
6847913004
50 mL in 1 POUCH (68479-130-04)

Annotations

UNII (FDA Substance ID)

15FIX9V2JP

TITANIUM DIOXIDE

RxCUI 38323

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "15FIX9V2JP",
    "rxcui": "38323",
    "inchikey": "SOQBVABWOPYFQZ-UHFFFAOYSA-N",
    "display_name": "TITANIUM DIOXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "692f9cda-eb6c-431f-a575-3778c6e12e3b": {
      "match": "brand_token",
      "title": "SKINPERFECT PRIMER SPF30 (ZINC OXIDE) LOTION [DERMALOGICA, LLC.]",
      "spl_version": "1",
      "published_date": "2024-04-29"
    }
  },
  "productid": "68479-130_adb2dff4-e406-4123-9624-2d0c12bcb6ef",
  "productndc": "68479-130",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "SkinPerfect Primer",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "part352",
  "marketing_category": "OTC MONOGRAPH FINAL",
  "nonproprietary_name": "Titanium Dioxide and Zinc Oxide",
  "start_marketing_date": "20120213",
  "active_numerator_strength": "40; 140"
}

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