MDP UV BIO SUNSCREEN

UNIISPL

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

Identification

ManufacturerSKINIDEA CO., LTD

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7222000302
1 TUBE in 1 CARTON (72220-003-02) / 40 mL in 1 TUBE (72220-003-01)

Annotations

UNII (FDA Substance ID)

V06SV4M95S

HOMOSALATE

RxCUI 91326

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "V06SV4M95S",
    "rxcui": "91326",
    "inchikey": "WSSJONWNBBTCMG-UHFFFAOYSA-N",
    "display_name": "HOMOSALATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "26db53cd-dd82-8790-e063-6394a90a92b1": {
      "match": "brand_token",
      "title": "MDP PEPTIDE 9 BIO SUN PRO (HOMOSALATE, OCTOCRYLENE, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE) STICK [SKINIDEA CO., LTD]",
      "spl_version": "3",
      "published_date": "2025-06-11"
    }
  },
  "productid": "72220-003_30877734-91d7-34c8-e063-6294a90a0e64",
  "productndc": "72220-003",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HOMOSALATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE",
  "proprietary_name": "MDP UV BIO SUNSCREEN",
  "active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ZINC OXIDE, HOMOSALATE, OCTOCRYLENE, OCTISALATE",
  "start_marketing_date": "20250301",
  "active_numerator_strength": "60; 45; 50; 103.8"
}

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