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United States · US · US:71874-080_29a6f565-5181-2a29-e063-6394a90a28e5
DAYCON Antibacterial Foaming Hand So ap
UNIISPLATC D08AE05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDaycon Products Company, Inc.
CountryUS (United States)
ATC codeD08AE05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1171874080421250 mL in 1 PACKAGE (71874-080-42)
Annotations
UNII (FDA Substance ID)
0F32U78V2Q
CHLOROXYLENOL
RxCUI 20877
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "0F32U78V2Q",
"rxcui": "20877",
"inchikey": "OSDLLIBGSJNGJE-UHFFFAOYSA-N",
"display_name": "CHLOROXYLENOL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"a37897d2-edfb-42f2-9a55-436965986512": {
"match": "brand_token",
"title": "DAYCON ANTIBACTERIAL FOAMING HAND SO AP (CHLOROXYLENOL) LIQUID [DAYCON PRODUCTS COMPANY, INC.]",
"spl_version": "5",
"published_date": "2024-12-23"
}
},
"productid": "71874-080_29a6f565-5181-2a29-e063-6394a90a28e5",
"productndc": "71874-080",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CHLOROXYLENOL",
"proprietary_name": "DAYCON Antibacterial Foaming Hand So ap",
"active_ingred_unit": "mg/100mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Chloroxylenol",
"start_marketing_date": "20110228",
"active_numerator_strength": ".3"
}Related drugs
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