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United States · US · US:51326-201_d4677ccd-57aa-437f-b862-58bb18b80028

Replenix Tinted Sunscreen

UNIISPLATC D02BA

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

Identification

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

Packs · 1

  • ndc11
    5132620101
    63 g in 1 BOTTLE (51326-201-01)

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": {
    "b60dc004-d713-47bc-a6e9-ea4783aa7019": {
      "match": "brand_token",
      "title": "REPLENIX LIP THERAPY HOMOSALATE (HOMOSALATE) LIPSTICK [TOPIDERM, INC.]",
      "spl_version": "7",
      "published_date": "2026-04-23"
    }
  },
  "productid": "51326-201_d4677ccd-57aa-437f-b862-58bb18b80028",
  "productndc": "51326-201",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTINOXATE; ZINC OXIDE",
  "proprietary_name": "Replenix Tinted Sunscreen",
  "active_ingred_unit": "mg/g; mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide and Octinoxate",
  "start_marketing_date": "20220422",
  "active_numerator_strength": "75; 145"
}

Related drugs

Other records sharing ATC code D02BA.

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