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United States · US · US:68062-2265_48dfd489-9f9b-ff51-e063-6294a90a25b0

Dr Lift Blemish

UNIISPLATC D01AE

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

Identification

ManufacturerSpa de Soleil
CountryUS (United States)
ATC codeD01AE
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6806222651
    100 mL in 1 BOTTLE (68062-2265-1)

Annotations

UNII (FDA Substance ID)
O414PZ4LPZ
SALICYLIC ACID
RxCUI 9525
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "O414PZ4LPZ",
    "rxcui": "9525",
    "inchikey": "YGSDEFSMJLZEOE-UHFFFAOYSA-N",
    "display_name": "SALICYLIC ACID",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "8abd6d8e-c69e-4374-ace8-d42b2d3e171e": {
      "match": "brand_token",
      "title": "DR SCHOLLS FUNGAL NAIL CLEAR AND CURE TOLNAFTATE ANTIFUNGAL (TOLNAFTATE) LIQUID [SCHOLL'S WELLNESS COMPANY LLC]",
      "spl_version": "4",
      "published_date": "2026-05-20"
    }
  },
  "productid": "68062-2265_48dfd489-9f9b-ff51-e063-6294a90a25b0",
  "productndc": "68062-2265",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SALICYLIC ACID; SULFUR",
  "proprietary_name": "Dr Lift Blemish",
  "active_ingred_unit": "mg/100mL; mg/100mL",
  "application_number": "M006",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "salicylic acid",
  "start_marketing_date": "20230627",
  "active_numerator_strength": "1; 2"
}

Related drugs

Other records sharing ATC code D01AE.

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