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United States · US · US:67777-141_275871a0-3173-c7fa-e063-6394a90ac014

Dynarex Povidone Iodine Prep Solution

UNIISPLATC D09AA09

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

Identification

ManufacturerDynarex Corporation
CountryUS (United States)
ATC codeD09AA09
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    6777714131
    48 BOTTLE in 1 CASE (67777-141-31) / 118 mL in 1 BOTTLE (67777-141-30)
  • ndc11
    6777714141
    24 BOTTLE in 1 CASE (67777-141-41) / 237 mL in 1 BOTTLE (67777-141-40)
  • ndc11
    6777714151
    24 BOTTLE in 1 CASE (67777-141-51) / 473 mL in 1 BOTTLE (67777-141-50)
  • ndc11
    6777714161
    4 BOTTLE in 1 CASE (67777-141-61) / 3790 mL in 1 BOTTLE (67777-141-60)

Annotations

UNII (FDA Substance ID)
85H0HZU99M
POVIDONE-IODINE
RxCUI 8611
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "85H0HZU99M",
    "rxcui": "8611",
    "inchikey": null,
    "display_name": "POVIDONE-IODINE",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "1e335cf8-eb08-40b4-abad-7a71bd2283d7": {
      "match": "brand_token",
      "title": "DYNAREX ANTIFUNGAL POWDER (MICONAZOLE) POWDER [DYNAREX CORPORATION]",
      "spl_version": "4",
      "published_date": "2024-11-22"
    }
  },
  "productid": "67777-141_275871a0-3173-c7fa-e063-6394a90ac014",
  "productndc": "67777-141",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "POVIDONE-IODINE",
  "proprietary_name": "Dynarex Povidone Iodine Prep Solution",
  "active_ingred_unit": "mg/mL",
  "application_number": "M003",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Povidone Iodine Prep Solution",
  "start_marketing_date": "20180508",
  "active_numerator_strength": "10"
}

Related drugs

Other records sharing ATC code D09AA09.

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