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United States · US · US:85339-212_45b3a9bc-1124-4545-e063-6394a90a5a58

Lip Protection

UNIISPL

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

Identification

ManufacturerTeton Dermatology Holdings, Inc.
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    8533921245
    1 CYLINDER in 1 CARTON (85339-212-45) / 4.5 g in 1 CYLINDER

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": {
    "a3e5819a-5132-9760-e053-2a95a90a058b": {
      "match": "brand_token",
      "title": "LIP SCREEN BROAD SPECTRUM SPF 40 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LIQUID [SUPERGOOP, LLC]",
      "spl_version": "7",
      "published_date": "2026-01-12"
    }
  },
  "productid": "85339-212_45b3a9bc-1124-4545-e063-6394a90a5a58",
  "productndc": "85339-212",
  "dosage_form": "STICK",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "Lip Protection",
  "active_ingred_unit": "mg/g; mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Titanium Dioxide, Zinc Oxide",
  "start_marketing_date": "20231027",
  "active_numerator_strength": "40; 55"
}

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