🇺🇸
United States · US · US:67777-308_2758dc6f-a18e-fc43-e063-6294a90aade6
Dynarex Green
UNIISPLATC D08AX08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDynarex Corporation
CountryUS (United States)
ATC codeD08AX08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11677773080359 mL in 1 BOTTLE (67777-308-03)
- ndc11677773081112 BOTTLE in 1 CASE (67777-308-11) / 473 mL in 1 BOTTLE (67777-308-01)
- ndc1167777308124 BOTTLE in 1 CASE (67777-308-12) / 3785 mL in 1 BOTTLE (67777-308-02)
Annotations
UNII (FDA Substance ID)
3K9958V90M
ALCOHOL
RxCUI 448
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "3K9958V90M",
"rxcui": "448",
"inchikey": "LFQSCWFLJHTTHZ-UHFFFAOYSA-N",
"display_name": "ALCOHOL",
"substance_type": "chemical",
"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": "67777-308_2758dc6f-a18e-fc43-e063-6294a90aade6",
"productndc": "67777-308",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALCOHOL",
"proprietary_name": "Dynarex Green",
"active_ingred_unit": "mL/mL",
"application_number": "M003",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "ALCOHOL",
"start_marketing_date": "20140701",
"active_numerator_strength": ".3"
}Related drugs
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