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United States · US · US:59088-299_23733118-0f3a-e4a8-e063-6394a90aa41e
GenRx Anti-Bacterial Gel
UNIISPLATC D08AX08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPureTek Corporation
CountryUS (United States)
ATC codeD08AX08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc115908829908118 mL in 1 BOTTLE, PUMP (59088-299-08)
- ndc115908829931500 mL in 1 BOTTLE, DISPENSING (59088-299-31)
- ndc115908829939710 mL in 1 BOTTLE, PUMP (59088-299-39)
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": {
"7d2827fd-b40f-454b-bb60-54d77823b18c": {
"match": "brand_token",
"title": "GENRX DAILY DEFENSE SKIN REPAIRING (DIMETHICONE) CREAM [PURETEK CORPORATION]",
"spl_version": "4",
"published_date": "2024-10-18"
}
},
"productid": "59088-299_23733118-0f3a-e4a8-e063-6394a90aa41e",
"productndc": "59088-299",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALCOHOL",
"proprietary_name": "GenRx Anti-Bacterial Gel",
"active_ingred_unit": "mL/100mL",
"application_number": "M014",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Alcohol",
"start_marketing_date": "20200318",
"active_numerator_strength": "62"
}Related drugs
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