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United States · US · US:55681-031_3ab4efb6-bd31-2583-e063-6294a90a415b

ProCure DryDrox

UNIISPLATC A02AB01

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

Identification

ManufacturerTwin Med LLC
CountryUS (United States)
ATC codeA02AB01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5568103104
    106 g in 1 TUBE (55681-031-04)

Annotations

UNII (FDA Substance ID)
5QB0T2IUN0
ALUMINUM HYDROXIDE
RxCUI 81948
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "5QB0T2IUN0",
    "rxcui": "81948",
    "inchikey": "WNROFYMDJYEPJX-UHFFFAOYSA-K",
    "display_name": "ALUMINUM HYDROXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "3d848ec8-5197-6d39-e063-6394a90aaef6": {
      "match": "brand_token",
      "title": "PROCURE FOAMING HAND SANITIZER (ETHYL ALCOHOL 72%) GEL [TWIN MED LLC]",
      "spl_version": "2",
      "published_date": "2026-06-01"
    }
  },
  "productid": "55681-031_3ab4efb6-bd31-2583-e063-6294a90a415b",
  "productndc": "55681-031",
  "dosage_form": "OINTMENT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALUMINUM HYDROXIDE",
  "proprietary_name": "ProCure DryDrox",
  "active_ingred_unit": "g/100g",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Aluminum Hydroxide Gel 2%",
  "start_marketing_date": "20250915",
  "active_numerator_strength": "2"
}

Related drugs

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