DRMTLGY Radiance Powder

UNIISPL

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

Identification

ManufacturerDRMTLGY

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8328619102
1 BOTTLE, WITH APPLICATOR in 1 CARTON (83286-191-02) / 6.5 g in 1 BOTTLE, WITH APPLICATOR (83286-191-01)

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": {
    "52be975c-6a2a-cf21-e063-6294a90a7c1d": {
      "match": "brand_token",
      "title": "DRMTLGY LIP SILK - SOFT (ZINC OXIDE) LOTION [DRMTLGY]",
      "spl_version": "1",
      "published_date": "2026-05-28"
    }
  },
  "productid": "83286-191_5256c59c-f503-c58c-e063-6294a90a3142",
  "productndc": "83286-191",
  "dosage_form": "POWDER",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "DRMTLGY Radiance Powder",
  "active_ingred_unit": "g/g; g/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Titanium dioxide, Zinc Oxide",
  "start_marketing_date": "20240318",
  "active_numerator_strength": ".125; .225"
}

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