ULTRA SOOTHER DRY-TOUCH SUNSCREEN

UNIISPL

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

Identification

Manufacturerskinnplus

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8753415002
1 TUBE in 1 BOX (87534-150-02) / 50 mL in 1 TUBE (87534-150-01)

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": {
    "52d4b1c1-7431-4f8c-e063-6294a90ad482": {
      "match": "brand_token",
      "title": "ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN BROAD SPECTRUM SPF 40 (ZINC OXIDE) CREAM [GRACE AND FIRE USA INC.]",
      "spl_version": "1",
      "published_date": "2026-05-29"
    }
  },
  "productid": "87534-150_4dbc1035-c41d-308c-e063-6394a90a36c4",
  "productndc": "87534-150",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HOMOSALATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE",
  "proprietary_name": "ULTRA SOOTHER DRY-TOUCH SUNSCREEN",
  "active_ingred_unit": "g/50mL; g/50mL; g/50mL; g/50mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE",
  "start_marketing_date": "20260324",
  "active_numerator_strength": "3; 2.25; 2.5; 5.19"
}

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