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United States · US · US:68062-2241_40d6a2ad-8650-9d41-e063-6394a90a380a

Dr Lift Antibacterial Body Wash

UNIISPLATC D08AJ01

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

Identification

ManufacturerSpa de Soleil
CountryUS (United States)
ATC codeD08AJ01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    6806222411
    240 mg in 1 TUBE (68062-2241-1)
  • ndc11
    6806222412
    60 mg in 1 TUBE (68062-2241-2)
  • ndc11
    6806222413
    100 mg in 1 TUBE (68062-2241-3)

Annotations

UNII (FDA Substance ID)
F5UM2KM3W7
BENZALKONIUM CHLORIDE
RxCUI 1379
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "F5UM2KM3W7",
    "rxcui": "1379",
    "inchikey": null,
    "display_name": "BENZALKONIUM CHLORIDE",
    "substance_type": "mixture",
    "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": "68062-2241_40d6a2ad-8650-9d41-e063-6394a90a380a",
  "productndc": "68062-2241",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BENZALKONIUM CHLORIDE",
  "proprietary_name": "Dr Lift Antibacterial Body Wash",
  "active_ingred_unit": "mg/240mg",
  "application_number": "M003",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "benzalkonium chloride",
  "start_marketing_date": "20200729",
  "active_numerator_strength": ".46"
}

Related drugs

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