NELLY DEVUYST BIOSOLAR COLORLIFT 3 TINTED SUNSCREEN

UNIISPL

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

Identification

ManufacturerLABORATOIRES DRUIDE INC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7144703301
1 TUBE in 1 BOX (71447-033-01) / 30 mL in 1 TUBE (71447-033-00)

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": {
    "19af4441-31b2-72db-e063-6394a90a813c": {
      "match": "brand_token",
      "title": "NELLY DEVUYST BIOSOLAR COLORLIFT 3 TINTED SUNSCREEN SPF30 (ZINC OXIDE) CREAM [LABORATOIRES DRUIDE INC]",
      "spl_version": "2",
      "published_date": "2026-01-16"
    }
  },
  "productid": "71447-033_485df439-ac26-fb36-e063-6394a90ad9f8",
  "productndc": "71447-033",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "NELLY DEVUYST BIOSOLAR COLORLIFT 3 TINTED SUNSCREEN",
  "active_ingred_unit": "g/100mL; g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE",
  "start_marketing_date": "20240527",
  "active_numerator_strength": "2; 18.4"
}

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