SKINSUIT LIP

UNIISPL

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

Identification

ManufacturerSkin Authority LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4600720511
3.2 g in 1 BOTTLE, WITH APPLICATOR (46007-205-11)

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": {
    "cb24d714-f6cd-4518-b146-627cfe6c2ccd": {
      "match": "brand_token",
      "title": "SKINSUIT LIP SPF 30 (ZINC OXIDE) GEL [SKIN AUTHORITY LLC]",
      "spl_version": "7",
      "published_date": "2025-12-22"
    }
  },
  "productid": "46007-205_4642868b-77bd-411e-e063-6394a90ac676",
  "productndc": "46007-205",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "SKINSUIT LIP",
  "active_ingred_unit": "g/100g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20200102",
  "active_numerator_strength": "10"
}

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