UV Skin Recovery SPF 50

UNIISPL

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

Identification

ManufacturerCP Skin Health Group, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7204303331
1 BOTTLE, PUMP in 1 CARTON (72043-0333-1) / 50.5 g in 1 BOTTLE, PUMP (72043-0333-2)

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": {
    "02e71602-13e1-43b3-9cba-a75e46cccacc": {
      "match": "brand_token",
      "title": "UV DAILY HYDRATION TINTED (OCTISALAT AND ZINC OXIDE SUNSCREEN) LOTION [CP SKIN HEALTH GROUP, INC]",
      "spl_version": "1",
      "published_date": "2026-05-20"
    }
  },
  "productid": "72043-0333_2874e1b3-83e7-91a6-e063-6294a90a9bb7",
  "productndc": "72043-0333",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ZINC OXIDE",
  "proprietary_name": "UV Skin Recovery SPF 50",
  "active_ingred_unit": "g/100g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide",
  "start_marketing_date": "20241113",
  "active_numerator_strength": "12.9"
}

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