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United States · US · US:72043-2530_cd1e2eda-ca7a-48a9-ab72-04e9aa639565

UV Clear Deep Tint

UNIISPLATC D02BA

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerCP Skin Health Group, Inc.
CountryUS (United States)
ATC codeD02BA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    7204325301
    50 g in 1 BOTTLE (72043-2530-1)
  • ndc11
    7204325302
    2 g in 1 PACKET (72043-2530-2)

Annotations

UNII (FDA Substance ID)
4Y5P7MUD51
OCTINOXATE
RxCUI 13369
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "4Y5P7MUD51",
    "rxcui": "13369",
    "inchikey": "YBGZDTIWKVFICR-JLHYYAGUSA-N",
    "display_name": "OCTINOXATE",
    "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": "72043-2530_cd1e2eda-ca7a-48a9-ab72-04e9aa639565",
  "productndc": "72043-2530",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTINOXATE; ZINC OXIDE",
  "proprietary_name": "UV Clear Deep Tint",
  "active_ingred_unit": "g/1000g; g/1000g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Octinoxate, Zinc Oxide Sunscreen",
  "start_marketing_date": "20240508",
  "active_numerator_strength": "750; 900"
}

Related drugs

Other records sharing ATC code D02BA.

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